Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 2
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 2
rs1274649
RAD51B
1.000 0.080 14 68207583 intron variant T/G snv 0.17 1
rs1316014
RAD51B
1.000 0.080 14 68232653 intron variant T/G snv 0.18 1
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 1
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2517388
ASH2L
0.925 0.080 8 38120214 intron variant T/G snv 0.24 1
rs3757322
CCDC170
1.000 0.080 6 151621059 3 prime UTR variant T/G snv 0.36 1
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 1
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 2
rs11820646 0.925 0.080 11 129591276 upstream gene variant T/C;G snv 1
rs199498
WNT3 ; LRRC37A2
0.925 0.120 17 46788237 intron variant T/C;G snv 1
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 1
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 2
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 2
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 2
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26 2
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 1
rs11196175
TCF7L2
0.925 0.160 10 112976855 intron variant T/C snv 0.20 1