Source: GWASCAT ×
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 35
rs1550532
DGKD
2 233356202 intron variant C/G snv 0.75 2
rs34339006
DGKD
1.000 0.040 2 233362876 intron variant C/T snv 0.32 2
rs3109133
GPR39
2 132545965 intron variant C/G;T snv 1
rs17265703
CSTA
3 122329797 intron variant A/G snv 0.12 2
rs10934582 3 122294507 downstream gene variant G/A snv 0.28 1
rs11918240
CASR
3 122226991 intron variant A/G;T snv 1
rs13068893 3 122307242 regulatory region variant C/G snv 8.7E-02 1
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 1
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 1
rs2270859
LOC105374071 ; PARP9
1.000 0.040 3 122536861 non coding transcript exon variant G/A snv 0.14 1
rs4678176
CASR
3 122290328 3 prime UTR variant A/G snv 9.1E-02 1
rs4678181 3 122320183 downstream gene variant G/A snv 8.6E-02 1
rs4685771
ITPR1 ; LOC105376933
3 4586857 intron variant C/T snv 0.20 1
rs13103813
DOK7
4 3466709 intron variant A/C snv 0.62 1
rs12517041 5 23301799 downstream gene variant A/G snv 0.15 1
rs11967485
ARID1B
6 156807123 intron variant G/A snv 0.15 1
rs17711722 7 65806210 downstream gene variant C/T snv 1
rs62462685
PHTF2
7 77879316 intron variant C/T snv 0.32 1
rs13301969 9 126532675 downstream gene variant C/T snv 0.33 1
rs10491003
LINC00709 ; LOC101928272
10 9286688 non coding transcript exon variant C/G;T snv 1
rs11101061 10 49244632 intergenic variant T/A snv 0.10 1
rs12780111
LOC101928272
10 9254687 regulatory region variant G/C snv 0.43 1
rs3750996
STIM1
1.000 0.040 11 4091970 3 prime UTR variant A/G snv 7.7E-03 1
rs7481584
CARS1
11 3007859 non coding transcript exon variant G/A snv 0.27 1