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
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs1232547491
RHCE
0.851 0.120 1 25385838 missense variant A/G snv 4
rs529365517
FLVCR1 ; FLVCR1-DT
0.925 0.080 1 212858540 missense variant C/T snv 3
rs886041906
CTLA4
0.882 0.200 2 203868002 stop gained G/A snv 6
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs373917450
XPC
0.925 0.160 3 14158365 missense variant G/T snv 4.0E-06 2
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1650697
MSH3 ; DHFR
0.925 0.120 5 80654962 missense variant A/G;T snv 0.86 3
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs1133400
INPP5A
1.000 0.080 10 132645884 missense variant A/G snv 0.22 0.18 4
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1126809
LOC107984363 ; TYR
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs876660725
ATM
1.000 0.080 11 108227859 synonymous variant A/C snv 1
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25