Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9942416 5 75741470 intergenic variant C/G snv 0.53 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
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 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
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs4953318
PRKCE
2 46127912 intron variant A/C snv 0.43 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 4
rs128494
CLDN14 ; LOC105369301
21 36461960 intron variant T/C snv 0.72 4
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12 4
rs2213169
HBE1 ; HBG2
11 5281833 intron variant G/A;T snv 4.2E-02 4
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4