Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9391858
TSBP1-AS1 ; TSBP1
0.925 0.080 6 32373621 intron variant A/G snv 0.13 6
rs3094609
HCG27
0.925 0.080 6 31197789 non coding transcript exon variant T/C snv 0.86 0.89 5
rs3130558
PSORS1C1
0.925 0.080 6 31129406 intron variant C/G snv 0.77 5
rs3130975
C6orf15 ; PSORS1C1
0.925 0.080 6 31114061 upstream gene variant C/T snv 0.27 5
rs3130981
CDSN ; PSORS1C1
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76 5
rs3131009
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs528878831
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs7382297
HLA-B
0.925 0.080 6 31279290 intron variant T/C;G snv 5
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 2
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs3130000
DHX16
1.000 0.080 6 30660305 non coding transcript exon variant A/G;T snv 2
rs4075958
RGS14
1.000 0.080 5 177357511 upstream gene variant G/A snv 0.21 2
rs4410871
PVT1
0.925 0.080 8 127802783 intron variant T/C snv 0.74 2
rs4713429
HCG22
1.000 0.080 6 31053240 upstream gene variant C/G snv 0.20 2
rs630923
CXCR5
1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 2
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 2
rs9260489
HLA-A
1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs9262615
HCG22
1.000 0.080 6 31053384 upstream gene variant C/G snv 0.21 2
rs9262635
HCG22
1.000 0.080 6 31057702 intron variant A/G snv 0.22 2
rs9262636
HCG22
1.000 0.080 6 31058071 intron variant A/G snv 0.22 2
rs10201872
SP140
1.000 0.080 2 230242009 intron variant C/T snv 0.13 1
rs10466829
CLECL1
1.000 0.080 12 9723495 intron variant G/A snv 0.55 1