Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1051226
TPM3
1 154157607 3 prime UTR variant G/A snv 1
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1052536
LIG3
0.776 0.200 17 35004556 3 prime UTR variant C/T snv 0.42 0.36 10
rs10786691
SUFU
0.925 0.160 10 102604895 intron variant G/A;T snv 3
rs10827337
PARD3
10 34202922 intron variant G/A snv 0.20 1
rs10925260
MTR
1 236884786 intron variant A/C snv 0.56 1
rs11247593
ARID1A
1 26725589 intron variant G/A snv 0.30 1
rs1141321
MMUT
6 49444720 missense variant C/G;T snv 0.32 1
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1169089134
FOLH1
0.790 0.320 11 49206785 missense variant C/G;T snv 9
rs1203798584
FOLR2
11 72221671 missense variant C/T snv 4.0E-06 1
rs1206846668
FOLH1
0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs1212671656
TUBGCP2
10 133297981 missense variant C/G snv 4.0E-06 1
rs12132032
PRKACB
1.000 0.080 1 84100906 intron variant A/G snv 0.41 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121918219
VANGL1
1.000 1 115682372 missense variant G/A snv 2.4E-05 4.2E-05 2
rs12218196
PARD3
10 34196864 intron variant T/C snv 2.0E-02 1
rs1237063529
CBS
0.752 0.360 21 43058894 missense variant T/G snv 5.6E-06 13
rs1256146
MTHFD1 ; ZBTB25
14 64453947 intron variant G/A snv 0.17 1
rs1257122540
SEC24B
4 109539620 missense variant C/G snv 7.0E-06 1
rs1268970749
PRCP
11 82838473 synonymous variant T/C snv 4.0E-06 1
rs1314974864
VANGL2
1 160419339 missense variant G/A snv 1.4E-05 1
rs1339039642
MTHFD1L
6 150905744 missense variant C/T snv 1.4E-05 2