Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61735836
FTCD-AS1 ; FTCD
21 46152973 missense variant C/T snv 5.7E-02 5.6E-02 3
rs1043673
NLRP2
19 55000864 missense variant C/A snv 0.37 0.39 2
rs9527
BORCS7-ASMT ; BORCS7
10 102863821 3 prime UTR variant C/T snv 0.21 2
rs11191979
GSTO1
10 104265109 intron variant T/C snv 0.23 1
rs113835371
XYLT2
17 50353660 missense variant G/A snv 9.3E-03 1.0E-02 1
rs12919719
CDH1
16 68788438 intron variant C/G snv 0.25 1
rs3790064
PNP
14 20472910 non coding transcript exon variant A/G;T snv 1
rs7196495
CDH1
16 68739957 intron variant C/G;T snv 1
rs7196661
CDH1
16 68740009 intron variant C/T snv 0.80 1
rs9989407 16 68730609 intergenic variant C/A;G;T snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104