Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs13239597
TNPO3 ; TPI1P2
0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 3
rs428073
TAOK3
1.000 0.080 12 118244946 missense variant C/G;T snv 0.72 3
rs6914831
AHI1
1.000 0.080 6 135318506 3 prime UTR variant C/T snv 0.59 0.59 3
rs77583790
IL12A-AS1
0.882 0.080 3 159976265 intron variant G/A;C snv 3
rs9373839
ATG5
0.882 0.080 6 106207742 intron variant T/C snv 0.15 3
rs10245867
JAZF1
0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 2
rs1028488 1.000 0.080 6 170281387 upstream gene variant G/T snv 0.46 2
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 2
rs1133906
SAMD9L
0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 2
rs11755393
UHRF1BP1
1.000 0.080 6 34856859 missense variant A/G;T snv 0.36 2
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 2
rs1887428
JAK2
1.000 0.080 9 4984530 5 prime UTR variant G/C;T snv 2
rs2066807
STAT2
0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 2
rs2176082
PXK
0.925 0.080 3 58345459 intron variant G/A snv 0.36 2
rs2275247
KIAA0319L
0.925 0.080 1 35442850 intron variant T/C snv 0.26 2
rs2732552
LOC105376626
0.925 0.080 11 35063045 regulatory region variant T/C snv 0.51 2
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 2
rs4850410
ANKRD44
1.000 0.080 2 197055445 intron variant C/G;T snv 2
rs6932056 0.925 0.080 6 137921300 intergenic variant T/C snv 3.4E-02 2
rs702814
JAZF1
1.000 0.080 7 28133113 intron variant C/T snv 0.37 2
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs7444
UBE2L3
1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32 2