Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
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
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
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
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
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
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs198833 6 26114280 downstream gene variant G/A snv 0.87 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 5