Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 1
rs11636802
LOC105370831
0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 1
rs11688943
PPIL3
1.000 0.120 2 200875545 intron variant T/C snv 0.30 1
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 1
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 1
rs1439287
ACOXL-AS1 ; ACOXL ; MIR4435-2HG
0.925 0.120 2 111114320 non coding transcript exon variant G/A snv 0.42 1
rs16976734
RFX7
0.925 0.120 15 56090097 3 prime UTR variant A/G snv 0.12 1
rs17246404
POT1
0.925 0.120 7 124822607 3 prime UTR variant C/A;T snv 1
rs2003869
LEF1
0.925 0.120 4 108105258 intron variant A/C;G;T snv 1
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 1
rs2147420
FAS
1.000 0.120 10 88999856 intron variant A/G snv 0.50 1
rs2236256
IPCEF1 ; OPRM1
0.925 0.120 6 154157305 3 prime UTR variant C/A snv 0.52 1
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 1
rs2466032
CASC19 ; PCAT1
1.000 0.120 8 127197575 non coding transcript exon variant T/C snv 0.23 1
rs2466035
PCAT1 ; CASC19
0.925 0.120 8 127198984 intron variant T/C snv 0.43 1
rs2511714 0.925 0.120 8 102566646 regulatory region variant T/G snv 0.41 1
rs2521269
TSPAN32 ; C11orf21
0.925 0.120 11 2299865 intron variant C/A;T snv 1
rs35748167 1.000 0.120 18 60370200 intron variant G/C;T snv 1
rs3769825
CASP8
0.925 0.120 2 201246657 intron variant A/G snv 0.46 1
rs3770745
QPCT
0.925 0.120 2 37368946 intron variant C/T snv 0.43 1
rs391023 0.925 0.120 16 85894208 upstream gene variant C/T snv 0.48 1
rs4368253 0.925 0.120 18 59955055 TF binding site variant T/A;C snv 1
rs4406737
FAS
0.925 0.120 10 88999967 intron variant A/G snv 0.50 1
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 1