Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1157198 3 166166211 upstream gene variant G/T snv 0.16 1
rs1157199 3 166166068 upstream gene variant G/A snv 0.16 1
rs1158519 3 166171330 intergenic variant T/C snv 0.28 1
rs11586632
RNPEP
1 201986486 intron variant G/A;T snv 1
rs11590299
RNPEP
1 201984468 intron variant T/A snv 0.55 1
rs11675251
ABI2
2 203384676 intron variant A/G snv 0.44 1
rs11675464
NBEAL1
2 203189019 intron variant A/G snv 0.43 1
rs11679740
RAPH1
2 203450671 intron variant G/A;C snv 1
rs11683935
RAPH1
2 203513148 intron variant C/G;T snv 1
rs11686036
ABI2
2 203376916 intron variant A/G;T snv 1
rs11687186
RAPH1
2 203455116 intron variant C/G snv 0.43 1
rs11690927
NBEAL1
2 203079305 intron variant A/G snv 0.44 1
rs11691351
WDR12
2 203009189 intron variant A/G snv 0.42 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 2
rs11693128
CYP20A1
2 203251178 intron variant A/G snv 0.44 1
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 4
rs11694728
ICA1L
2 202801596 intron variant T/G snv 0.39 1
rs11706636 3 166115849 intergenic variant A/G snv 0.45 1
rs11711013 3 165719779 intron variant T/G snv 0.32 1
rs11715356 3 166051370 intergenic variant C/A;G;T snv 1
rs11720167 3 165768357 intron variant T/A;G snv 1
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs1174604 2 203556561 intergenic variant T/C snv 0.26 1
rs1174605 2 203556781 intergenic variant T/A;C snv 1