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
rs769031989
STAT3
0.851 0.160 17 42322464 missense variant T/A snv 7.0E-06 4
rs756966085
DLC1
0.882 0.080 8 13090431 missense variant C/T snv 8.0E-06 7.0E-06 4
rs745501336
RAB43 ; ISY1-RAB43
0.882 0.080 3 129091263 missense variant C/T snv 4.6E-05 7.0E-06 3
rs1476081557
KMT2B
0.882 0.080 19 35721455 missense variant G/T snv 7.0E-06 3
rs779555087
HNF4A
0.882 0.080 20 44414561 missense variant A/G snv 1.6E-05 1.4E-05 3
rs372894000
DLC1
0.882 0.080 8 13092766 missense variant C/T snv 2.0E-05 1.4E-05 4
rs764555290
KRT6A
0.882 0.080 12 52492759 missense variant G/C snv 1.2E-05 1.4E-05 3
rs367597251
MDM2
0.807 0.080 12 68839587 missense variant A/G snv 1.5E-04 5.1E-04 10
rs80309960
XRCC5
0.851 0.080 2 216122110 missense variant T/A snv 3.5E-04 1.1E-03 4
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3734091
XRCC4
0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 19
rs12732894
ARHGEF10L
0.882 0.080 1 17582733 intron variant G/A snv 1.6E-02 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs145204276
ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135