Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10491003
LINC00709 ; LOC101928272
10 9286688 non coding transcript exon variant C/G;T snv 2
rs12150338
WDR81
17 1730810 synonymous variant C/G;T snv 4.0E-06; 0.12 2
rs1402200 3 122303570 intergenic variant G/A;C snv 2
rs16833078
CCDC58
3 122380747 intron variant A/G;T snv 2
rs16833080
CCDC58
3 122382060 intron variant C/A;T snv 2
rs16833168
LOC105374071 ; PARP9
3 122535800 3 prime UTR variant C/A;G;T snv 2
rs17200894
FAM162A
3 122411294 3 prime UTR variant C/G;T snv 2
rs17711722 7 65806210 downstream gene variant C/T snv 2
rs3792289
CASR
3 122274753 intron variant A/G;T snv 2
rs17266816
FAM162A
3 122410027 3 prime UTR variant G/A snv 7.6E-02 2
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 2
rs17265703
CSTA
3 122329797 intron variant A/G snv 0.12 4
rs2001548 3 122313942 upstream gene variant G/A snv 0.12 2
rs5008830 3 122311615 intergenic variant G/A snv 0.12 2
rs9789994
KPNA1
3 122499004 intron variant T/A snv 0.13 2
rs17201246
KPNA1 ; LOC102723582
3 122426623 3 prime UTR variant C/A snv 0.13 2
rs2270859
LOC105374071 ; PARP9
1.000 0.040 3 122536861 non coding transcript exon variant G/A snv 0.14 2
rs17267388
PARP9 ; LOC105374071
3 122548699 intron variant G/A snv 0.14 2
rs11929034
PARP9 ; LOC105374071
3 122560202 intron variant G/A snv 0.14 2
rs11967485
ARID1B
6 156807123 intron variant G/A snv 0.15 2
rs1067
WDR5B
3 122414118 3 prime UTR variant G/A snv 0.16 2
rs7336933
LOC105370176
13 41984940 downstream gene variant G/A snv 0.17 2
rs4491840
CCDC58
3 122361900 intron variant G/A snv 0.17 2
rs16832956 3 122298661 regulatory region variant C/G;T snv 0.19 2