Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
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
rs10810657 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 7
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 7
rs1129038
HERC2
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50 6
rs1800407
OCA2
0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 5
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 4
rs4268748
DEF8
0.925 0.080 16 89960104 intron variant T/C snv 0.30 3
rs12931267
FANCA
1.000 0.040 16 89752324 intron variant C/G snv 4.7E-02 3
rs35063026
SPATA33
0.925 0.080 16 89669749 3 prime UTR variant C/T snv 4.7E-02 3
rs1667392
HERC2
15 28288419 intron variant G/A;C;T snv 2
rs1110400
MC1R
1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 2
rs1805005
MC1R
0.827 0.080 16 89919436 missense variant G/T snv 8.6E-02 8.0E-02 2
rs1805008
MC1R
0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 2
rs183671
SLC45A2
1.000 0.040 5 33964105 intron variant T/A;G snv 2
rs10519170 15 48393978 regulatory region variant A/G snv 0.18 1
rs1834640 15 48099968 intergenic variant A/G snv 0.29 1
rs2675345 15 48108002 intergenic variant A/G;T snv 1
rs6142102 20 34116821 upstream gene variant C/G snv 0.60 1
rs6602665 10 13563982 intergenic variant T/C snv 8.2E-02 1
rs6602666 10 13564490 intergenic variant A/G snv 8.3E-02 1
rs79592764 3 187681148 intergenic variant C/T snv 2.7E-02 1