Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs2845885
FLRT1 ; MACROD1
11 64101590 intron variant C/T snv 0.87 5
rs438811
APOC1
19 44913484 non coding transcript exon variant C/T snv 0.29 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 5
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4