Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10001545 4 87254878 intergenic variant C/A;T snv 3
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs10787429
GPAM
10 112189906 intron variant T/A;C snv 2
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 3
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11124554
STRN
2 36922355 intron variant T/A;C snv 2
rs111532669
PTCH1
9 95446682 3 prime UTR variant C/T snv 1.8E-02 2
rs11597390 10 100101678 downstream gene variant G/A snv 0.29 4
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 5
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 4
rs12500824
SHROOM3
1.000 0.040 4 76495474 intron variant A/G;T snv 3
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs13077101
RABL3
3 120706484 intron variant T/C snv 4
rs13247499
JAZF1
7 28139639 intron variant C/A snv 0.10 2
rs13395911
EFHD1
2 232655544 intron variant A/T snv 0.59 3
rs144104656 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 3
rs144983009 5 56792072 intergenic variant C/T snv 5.7E-02 2
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs149940960
GREB1
1.000 0.120 2 11641492 3 prime UTR variant T/C snv 1.0E-02 3
rs1583686 5 85922051 intergenic variant T/C snv 0.79 3
rs1658972 9 6665010 intron variant C/A;T snv 2
rs16840760 2 204118831 intergenic variant T/C snv 3.6E-02 4
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6