Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9379832 1.000 0.080 6 26185972 downstream gene variant A/G snv 0.26 3
rs11055034
APOLD1 ; LOC107984129
1.000 0.080 12 12737692 intron variant C/A;T snv 2
rs2274224
PLCE1-AS1 ; PLCE1
0.882 0.080 10 94279840 missense variant G/A;C snv 8.8E-05; 0.44 2
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 2
rs2280235
STAT1
1.000 0.080 2 190979104 splice region variant A/G snv 0.23 1
rs4432842 1.000 0.080 5 57876251 intergenic variant T/C snv 0.45 1
rs61862780 1.000 0.080 10 92708886 downstream gene variant T/C snv 0.39 1
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 4
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs4932373
FES
1.000 0.040 15 90886057 intron variant A/C snv 0.25 2
rs222857
CLDN7
1.000 0.040 17 7261244 intron variant C/A;G;T snv 0.52 1
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 4
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 4
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs2229742
NRIP1
21 14966851 missense variant G/C snv 7.9E-02 7.1E-02 3