Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs11672660
GIPR ; MIR642B
19 45676926 intron variant C/T snv 0.18 0.17 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 4
rs12055786
RGS17
6 153109990 intron variant C/T snv 0.46 3
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs4869272
MIR583HG ; LOC101929710
5 96203744 intron variant C/T snv 0.72 3
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs10278336
YKT6
7 44205764 intron variant A/C;G snv 2
rs10500292
SYMPK
19 45824675 intron variant C/T snv 0.46 2
rs10747083 12 132465032 downstream gene variant G/A;T snv 2
rs11039119
MIR6745 ; PACSIN3
11 47180373 intron variant G/A snv 0.38 0.33 2
rs11039130 11 47207765 intergenic variant C/T snv 0.20 2
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs1124649
TMEM214
2 27037601 missense variant G/A snv 0.32 0.35 2
rs11607883 11 45818158 intron variant G/A snv 0.40 2
rs11619319
PLUT
13 27913462 intron variant A/G snv 0.23 2
rs11715915
AMT
3 49417897 synonymous variant C/A;T snv 0.28 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs11891554
PPM1G
2 27390750 intron variant G/A;T snv 7.1E-02 2