Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12714207
LOC105374852
2 88016274 upstream gene variant C/T snv 0.62 2
rs2885493 2 88006827 upstream gene variant T/A;C snv 2
rs17665859
TDRP
8 495601 intron variant T/C snv 5.9E-02 2
rs16928809
SLC22A18
11 2915722 intron variant G/A;T snv 3
rs12206204
H2BC4
6 26116754 intron variant C/T snv 1.1E-02 2
rs17868378 2 233899733 intergenic variant A/C;G snv 2
rs10164928 2 233893139 regulatory region variant C/T snv 5.8E-02 2
rs28900731 2 233881465 intergenic variant A/G snv 0.13 2
rs11890203 2 233871485 upstream gene variant A/G snv 0.14 2
rs13390675
MSL3P1
2 233868106 non coding transcript exon variant G/C snv 7.1E-02 2
rs13384181
MSL3P1
2 233866700 non coding transcript exon variant G/A snv 6.5E-02 5.9E-02 2
rs13416326
HJURP
2 233836015 intron variant A/G snv 7.2E-02 2
rs2270856
MROH2A
2 233833162 missense variant C/T snv 7.7E-02 7.2E-02 2
rs879665
MROH2A
2 233831490 missense variant G/A snv 0.15 0.17 2
rs2361507
MROH2A
2 233831164 intron variant T/G snv 0.23 2
rs988344
MROH2A
2 233812088 intron variant A/C;T snv 2
rs11674078
MROH2A
2 233809878 intron variant T/C snv 0.18 2
rs2041651
MROH2A
2 233805166 intron variant G/T snv 0.85 2
rs6716168
MROH2A
2 233804783 intron variant C/G;T snv 2
rs10175949
MROH2A
2 233804275 intron variant G/A snv 0.89 2
rs730673
MROH2A
2 233803031 intron variant G/A;C snv 2
rs17862891
MROH2A
2 233801637 intron variant G/A snv 9.1E-05 2
rs11678741
MROH2A
2 233801185 intron variant C/G snv 0.14 2
rs11563069
MROH2A
2 233799924 intron variant G/A snv 0.75 0.79 2
rs13013882
MROH2A
2 233799782 splice region variant G/A snv 0.70 0.72 2