Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 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
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs6504074
BRIP1
0.882 0.120 17 61822429 intron variant G/A;T snv 6
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 6
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs2236496
RCL1
9 4844265 intron variant T/C snv 0.19 5
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 5
rs4449583
TERT
5 1284020 intron variant C/T snv 0.25 5