Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5030868
G6PD
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5