Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1550532
DGKD
2 233356202 intron variant C/G snv 0.75 4
rs17265703
CSTA
3 122329797 intron variant A/G snv 0.12 4
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 3
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 2
rs10491003
LINC00709 ; LOC101928272
10 9286688 non coding transcript exon variant C/G;T snv 2
rs1067
WDR5B
3 122414118 3 prime UTR variant G/A snv 0.16 2
rs10934578
CASR
0.925 0.080 3 122258435 intron variant G/T snv 0.30 2
rs10934582 3 122294507 downstream gene variant G/A snv 0.28 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
rs12107092
FAM162A
3 122405001 intron variant C/T snv 0.19 2
rs12635478
CASR
3 122289706 3 prime UTR variant C/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
rs13095172
CASR
3 122271410 intron variant C/T 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
rs1570669
CYP24A1
0.925 0.080 20 54157888 intron variant A/G snv 0.42 2
rs16832956 3 122298661 regulatory region variant C/G;T snv 0.19 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