Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs373917450
XPC
0.925 0.160 3 14158365 missense variant G/T snv 4.0E-06 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs41556519
ERCC2
0.807 0.400 19 45352352 missense variant G/A snv 6.0E-05 2.8E-05 6
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs529365517
FLVCR1 ; FLVCR1-DT
0.925 0.080 1 212858540 missense variant C/T snv 3
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs876660725
ATM
1.000 0.080 11 108227859 synonymous variant A/C snv 1
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs886041906
CTLA4
0.882 0.200 2 203868002 stop gained G/A snv 6
rs897453
PEMT
1.000 0.080 17 17522317 missense variant C/A;G;T snv 8.0E-06; 0.34 2