Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs11021221 11 95575690 intron variant T/A;G snv 4
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs13191659
LINC00240
6 27033276 intron variant C/G;T snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs4712656
CASC15 ; NBAT1
1.000 0.040 6 22136033 non coding transcript exon variant G/A;C snv 4
rs4968782 1.000 0.080 17 63471115 upstream gene variant G/A;T snv 4