Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs2274976
MTHFR
0.807 0.320 1 11790870 missense variant C/T snv 5.6E-02 4.2E-02 7
rs12132032
PRKACB
1.000 0.080 1 84100906 intron variant A/G snv 0.41 2
rs121918219
VANGL1
1.000 1 115682372 missense variant G/A snv 2.4E-05 4.2E-05 2
rs761123443
VANGL1
1.000 1 115663998 missense variant G/A snv 2.4E-05 6.3E-05 2
rs1051226
TPM3
1 154157607 3 prime UTR variant G/A snv 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
rs1314974864
VANGL2
1 160419339 missense variant G/A snv 1.4E-05 1
rs148512517
VANGL1
1 115691354 missense variant G/A;T snv 5.2E-05 1
rs150198234
MTR
1 236852992 synonymous variant G/A snv 4.0E-06 1.4E-05 1
rs34059106
VANGL1
1 115684037 missense variant A/C;G snv 4.0E-03; 4.0E-06 1.7E-02 1
rs4839469
VANGL1
1 115663802 missense variant G/A;C snv 0.15 1
rs573558988
VANGL2
1 160420419 missense variant G/A;T snv 8.0E-06 8.4E-05 1
rs594631
PRKACB ; LOC107985046
1 84220882 intron variant A/T snv 0.31 1
rs751839046
MTR
1 236859890 missense variant G/A snv 4.0E-06 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs2544390
LRP2
0.925 0.080 2 169348336 intron variant C/T snv 0.45 4