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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs143396368
FXN
0.807 0.200 9 69072623 missense variant G/A;C snv 3.2E-05; 8.0E-06 7
rs104894107
FXN
0.882 0.160 9 69064942 missense variant G/C;T snv 3.6E-05; 2.8E-05 6
rs142157346
FXN
0.882 0.160 9 69053240 missense variant G/T snv 4
rs104894105
FXN
0.925 0.120 9 69053193 stop gained T/C;G snv 1.2E-05 2
rs104894106
FXN
0.925 0.120 9 69065013 missense variant A/G;T snv 4.0E-06 2
rs138034837
FXN
0.925 0.120 9 69072622 missense variant C/T snv 2
rs138471431
FXN
0.925 0.120 9 69065016 missense variant T/C snv 2
rs104894108
FXN
1.000 0.120 9 69035785 start lost G/A;T snv 9.1E-06 1
rs139616452
FXN
1.000 0.120 9 69072673 missense variant C/T snv 1
rs140987490
FXN
1.000 0.120 9 69064936 splice acceptor variant A/G snv 1
rs141935559
FXN
1.000 0.120 9 69035936 frameshift variant C/-;CC delins 1
rs144104124
FXN
1.000 0.120 9 69072722 missense variant T/G snv 1
rs146818694
FXN
1.000 0.120 9 69064991 missense variant C/G snv 1
rs148443992
FXN
1.000 0.120 9 69072686 missense variant T/G snv 1
rs56214919
FXN
1.000 0.120 9 69072646 missense variant T/G snv 1
rs886037630
FXN
1.000 0.120 9 69053247 protein altering variant ATGTCT/TACACCTTGAGGACA delins 1