rs_ID |
Location |
Functional Annotation |
rs2268206 |
Chr21:31039378(Fwd) |
intron_variant; nc_transcript_variant |
rs363522 |
Chr21:31023226(Fwd) |
intron_variant; nc_transcript_variant |
rs9981377 |
Chr21:31030797(Fwd) |
intron_variant; nc_transcript_variant |
rs363564 |
Chr21:31035432(Fwd) |
intron_variant; nc_transcript_variant |
rs363544 |
Chr21:31050277(Fwd) |
intron_variant; nc_transcript_variant |
rs9977239 |
Chr21:23382128(Fwd) |
intron_variant; nc_transcript_variant |
rs9983438 |
Chr21:23380208(Fwd) |
downstream_gene_variant |
rs9984244 |
Chr21:23380362(Fwd) |
downstream_gene_variant |
rs9975984 |
Chr21:23380533(Fwd) |
downstream_gene_variant |
rs9983814 |
Chr21:23380592(Fwd) |
downstream_gene_variant |
rs2827210 |
Chr21:23381459(Fwd) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs1557284 |
Chr21:23382284(Fwd) |
intron_variant; nc_transcript_variant |
rs1557286 |
Chr21:23382663(Fwd) |
intron_variant; nc_transcript_variant |
rs1571652 |
Chr21:23383038(Fwd) |
intron_variant; nc_transcript_variant |
rs1571654 |
Chr21:23383078(Fwd) |
intron_variant; nc_transcript_variant |
rs1571655 |
Chr21:23383104(Fwd) |
intron_variant; nc_transcript_variant |
rs9982612 |
Chr21:23383401(Fwd) |
intron_variant; nc_transcript_variant |
rs9306044 |
Chr21:23383454(Fwd) |
intron_variant; nc_transcript_variant |
rs4315619 |
Chr21:23386382(Fwd) |
intron_variant; nc_transcript_variant |
rs4459807 |
Chr21:23386446(Fwd) |
intron_variant; nc_transcript_variant |
rs10470233 |
Chr21:23386551(Fwd) |
intron_variant; nc_transcript_variant |
rs9653766 |
Chr21:23387605(Fwd) |
intron_variant; nc_transcript_variant |
rs9306045 |
Chr21:23388794(Fwd) |
intron_variant; nc_transcript_variant |
rs2186427 |
Chr21:23388942(Fwd) |
intron_variant; nc_transcript_variant |
rs1573450 |
Chr21:23391068(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1573451 |
Chr21:23391186(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1573452 |
Chr21:23391277(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs989273 |
Chr21:23392648(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9974295 |
Chr21:23393284(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9978097 |
Chr21:23394301(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17004094 |
Chr21:23395334(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2027620 |
Chr21:23395679(Fwd) |
feature_truncation; intron_variant; nc_transcript_variant |
rs9981393 |
Chr21:23396028(Fwd) |
intron_variant; nc_transcript_variant |
rs17004095 |
Chr21:23396682(Fwd) |
intron_variant; nc_transcript_variant |
rs9975680 |
Chr21:23397171(Fwd) |
intron_variant; nc_transcript_variant |
rs9306049 |
Chr21:23397513(Fwd) |
intron_variant; nc_transcript_variant |
rs2051375 |
Chr21:23397690(Fwd) |
feature_truncation; intron_variant; nc_transcript_variant |
rs9977426 |
Chr21:23398004(Fwd) |
intron_variant; nc_transcript_variant |
rs13353380 |
Chr21:23398255(Fwd) |
intron_variant; nc_transcript_variant |
rs914237 |
Chr21:46749718(Fwd) |
|
rs9306050 |
Chr21:23398592(Fwd) |
intron_variant; nc_transcript_variant |
rs957794 |
Chr21:46758766(Fwd) |
downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs9306051 |
Chr21:23398731(Fwd) |
intron_variant; nc_transcript_variant |
rs9637167 |
Chr21:46759886(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9984201 |
Chr21:23401983(Fwd) |
intron_variant; nc_transcript_variant |
rs9637195 |
Chr21:46756999(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9982902 |
Chr21:23405006(Fwd) |
intron_variant; nc_transcript_variant |
rs9637196 |
Chr21:46757080(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9982988 |
Chr21:23405043(Fwd) |
intron_variant; nc_transcript_variant |
rs2246417 |
Chr21:46759503(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9976674 |
Chr21:23411627(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7278329 |
Chr21:23415818(Fwd) |
intron_variant; nc_transcript_variant |
rs9983993 |
Chr21:23416839(Fwd) |
intron_variant; nc_transcript_variant |
rs9981341 |
Chr21:23416914(Fwd) |
intron_variant; nc_transcript_variant |
rs9984043 |
Chr21:23419371(Fwd) |
intron_variant; nc_transcript_variant |
rs9985062 |
Chr21:23419788(Fwd) |
intron_variant; nc_transcript_variant |
rs9979200 |
Chr21:23420154(Fwd) |
intron_variant; nc_transcript_variant |
rs9979224 |
Chr21:23420223(Fwd) |
intron_variant; nc_transcript_variant |
rs9976016 |
Chr21:23420396(Fwd) |
intron_variant; nc_transcript_variant |
rs9982425 |
Chr21:23421133(Fwd) |
intron_variant; nc_transcript_variant |
rs11088903 |
Chr21:23425157(Fwd) |
intron_variant; nc_transcript_variant |
rs9984961 |
Chr21:23426541(Fwd) |
intron_variant; nc_transcript_variant |
rs958335 |
Chr21:23427794(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11088905 |
Chr21:23429292(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9979179 |
Chr21:23433540(Fwd) |
intron_variant; nc_transcript_variant |
rs9980397 |
Chr21:23437554(Fwd) |
intron_variant; nc_transcript_variant |
rs9976697 |
Chr21:23439274(Fwd) |
intron_variant; nc_transcript_variant |
rs9976390 |
Chr21:23439314(Fwd) |
intron_variant; nc_transcript_variant |
rs17004105 |
Chr21:23441086(Fwd) |
intron_variant; nc_transcript_variant |
rs17004107 |
Chr21:23444685(Fwd) |
intron_variant; nc_transcript_variant |
rs9985055 |
Chr21:23445840(Fwd) |
intron_variant; nc_transcript_variant |
rs1571653 |
Chr21:23383051(Fwd) |
intron_variant; nc_transcript_variant |