Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10934582 3 122294507 downstream gene variant G/A snv 0.28 2
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 2
rs13085498 3 122292516 downstream gene variant C/A;T snv 0.28 2
rs13085674 3 122292504 downstream gene variant G/A snv 0.28 2
rs1402200 3 122303570 intergenic variant G/A;C snv 2
rs1472621 3 122293879 downstream gene variant A/G snv 0.28 2
rs16832956 3 122298661 regulatory region variant C/G;T snv 0.19 2
rs17711722 7 65806210 downstream gene variant C/T snv 2
rs2001548 3 122313942 upstream gene variant G/A snv 0.12 2
rs4678180 3 122318950 downstream gene variant T/C snv 0.62 2
rs5008830 3 122311615 intergenic variant G/A snv 0.12 2
rs6438720 3 122298385 TF binding site variant A/C snv 0.60 2
rs6803098 3 122321763 upstream gene variant C/T snv 0.62 2
rs9851884 3 122301347 regulatory region variant A/G snv 0.66 2
rs9864290 3 122321215 upstream gene variant C/T snv 0.62 2
rs11967485
ARID1B
6 156807123 intron variant G/A snv 0.15 2
rs7481584
CARS1
11 3007859 non coding transcript exon variant G/A snv 0.27 2
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 2
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 2
rs12635478
CASR
3 122289706 3 prime UTR variant C/A snv 0.28 2
rs13095172
CASR
3 122271410 intron variant C/T snv 0.28 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs3749203
CASR
3 122257647 intron variant C/T snv 0.45 2
rs3749208
CASR
3 122261437 intron variant C/T snv 0.28 2