Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033690
GALT
0.882 0.120 9 34647858 missense variant C/G;T snv 4.0E-06; 2.5E-04 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121918474
PROS1
0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 11
rs1252641479
ARHGEF7
1.000 0.040 13 111300800 missense variant T/G snv 4.0E-06 2
rs1286080173
ATP7B
0.925 0.160 13 51942551 missense variant G/A;C snv 8.0E-06; 4.0E-06 2
rs1366026966
ATP7B
1.000 0.040 13 51939100 missense variant A/T snv 7.0E-06 1
rs149989682
ABCA3
0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 10
rs1566304640
EDNRB-AS1 ; EDNRB
0.827 0.280 13 77900593 missense variant G/A snv 8
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs200134167
DUOX2
1.000 0.040 15 45108105 missense variant C/T snv 2.5E-04 2.2E-04 1
rs35457250
AHSG
0.925 0.080 3 186620775 missense variant C/T snv 9.0E-03 8.1E-03 5
rs376910645
ATP7B
0.925 0.160 13 51944162 missense variant C/T snv 4.0E-06 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs587782995
PURA
0.708 0.360 5 140114480 missense variant T/C snv 42
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs70961709
AHSG
1.000 0.040 3 186620652 missense variant G/A;C snv 4.0E-06; 4.0E-06 3
rs749085322
ATP7B
0.925 0.160 13 51941132 missense variant T/C snv 4.0E-05 2.1E-05 2
rs755153760
NUP214
1.000 0.040 9 131144504 missense variant G/A snv 1.6E-04 2.1E-05 1
rs761234173
CDH13
1.000 0.040 16 83783345 missense variant G/A snv 4.0E-06 2
rs762143558
IGSF1
1.000 0.040 X 131277876 missense variant G/A snv 9.3E-05 9.5E-06 1
rs769214
CAT
0.925 0.160 11 34438170 upstream gene variant G/A snv 0.61 2
rs775541743
ATP7B
0.925 0.160 13 51942481 missense variant A/T snv 4.0E-06 2
rs781214034
EDNRB ; EDNRB-AS1
0.790 0.320 13 77903538 missense variant C/T snv 1.3E-04 2.8E-05 10