Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519719
BRAF
1.000 0.080 7 140781593 missense variant T/C snv 2
rs1057520015
ROCK1
1.000 0.080 18 20955181 missense variant G/A snv 2
rs34158769
LOC107986582
1.000 0.080 6 26336344 upstream gene variant G/A snv 8.2E-02 2
rs36162392
LOC105374988
1.000 0.080 6 26568907 upstream gene variant T/A;C;G snv 2
rs4886591
ADAMTS7
1.000 0.080 15 78782176 intron variant G/A;C snv 2
rs80264589
LINC00240
1.000 0.080 6 26959823 intron variant G/A snv 7.0E-02 2
rs10436951
CEP170
1.000 0.080 1 243199378 intron variant A/G snv 7.1E-02 1
rs1057520037
EGFR
1.000 0.080 7 55174782 missense variant G/C snv 1
rs11008347
MALRD1
1.000 0.080 10 19072094 intron variant C/G snv 0.12 1
rs114002231 1.000 0.080 6 31459618 intron variant G/C snv 1
rs114385935
LOC105374996 ; LINC00533
1.000 0.080 6 28651576 upstream gene variant A/G snv 1
rs114393147 1.000 0.080 6 33157965 downstream gene variant A/G snv 1
rs114601353 1.000 0.080 6 30389517 intergenic variant C/T snv 1
rs114828403 1.000 0.080 6 32809144 downstream gene variant T/C snv 1
rs115100928 1.000 0.080 6 32419655 intergenic variant G/A snv 1
rs11514963
MKLN1
1.000 0.080 7 131247904 intron variant C/T snv 0.81 1
rs115287935
ZNF311
1.000 0.080 6 29006488 upstream gene variant G/T snv 1
rs115613607 1.000 0.080 6 32413503 regulatory region variant G/C snv 1
rs115666025
MUC22
1.000 0.080 6 31009903 upstream gene variant G/A snv 1
rs115729734
HLA-A
1.000 0.080 6 29931238 upstream gene variant T/C;G snv 1
rs115819854 1.000 0.080 6 32683864 intergenic variant G/T snv 1
rs115870917 1.000 0.080 6 29639324 upstream gene variant T/C snv 1
rs116165775
ETAA1
1.000 0.080 2 67400580 3 prime UTR variant G/A;T snv 1
rs116260619 1.000 0.080 6 30479897 intergenic variant A/C snv 1
rs116295105
PPP1R18
1.000 0.080 6 30685004 missense variant C/G;T snv 1