Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 11
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 10
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 9
rs1126809
LOC107984363 ; TYR
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 8
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 6
rs35407
SLC45A2
0.807 0.080 5 33946466 3 prime UTR variant A/C;G snv 6
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs663743
LOC102723878 ; CCDC88B
0.827 0.120 11 64340263 5 prime UTR variant G/A snv 0.33 0.25 5
rs9419958
STN1
0.851 0.040 10 103916188 intron variant T/C snv 0.75 5
rs10424978 0.851 0.080 19 4837545 upstream gene variant C/A;G snv 4
rs1246946 0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34 4
rs4761496 0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23 4
rs6707137 0.882 0.040 2 88254832 regulatory region variant G/A snv 0.12 4
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs3769823
CASP8
0.851 0.040 2 201258272 missense variant A/G snv 0.66 0.65 4
rs117744081
CPVL
0.851 0.080 7 29092663 missense variant A/G snv 2.2E-02 2.3E-02 4
rs2289702
CTSH
0.851 0.120 15 78944951 missense variant C/T snv 9.3E-02 7.8E-02 4