Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805009
MC1R ; TUBB3
0.790 0.280 16 89920138 missense variant G/A;C snv 4.0E-06; 9.1E-03 9
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs886041906
CTLA4
0.882 0.200 2 203868002 stop gained G/A snv 6
rs41556519
ERCC2
0.807 0.400 19 45352352 missense variant G/A snv 6.0E-05 2.8E-05 6
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs1133400
INPP5A
1.000 0.080 10 132645884 missense variant A/G snv 0.22 0.18 4
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
rs1650697
MSH3 ; DHFR
0.925 0.120 5 80654962 missense variant A/G;T snv 0.86 3
rs2278952
PEMT
1.000 0.080 17 17582270 5 prime UTR variant G/A snv 5.4E-02 2
rs897453
PEMT
1.000 0.080 17 17522317 missense variant C/A;G;T snv 8.0E-06; 0.34 2
rs373917450
XPC
0.925 0.160 3 14158365 missense variant G/T snv 4.0E-06 2
rs876660725
ATM
1.000 0.080 11 108227859 synonymous variant A/C snv 1