Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 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
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 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
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
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 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
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5