Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121912811
rs121912811
CYP11A1
1 1.000 15 74345103 missense variant G/A snv 0.800 1.000 5 2001 2009
dbSNP: rs121912812
rs121912812
CYP11A1
1 1.000 15 74339668 missense variant G/A snv 3.2E-05 0.800 1.000 5 2001 2009
dbSNP: rs121912813
rs121912813
CYP11A1
1 1.000 15 74347903 missense variant A/C snv 0.800 1.000 5 2001 2009
dbSNP: rs121912814
rs121912814
CYP11A1
1 1.000 15 74338761 missense variant A/T snv 4.0E-06 0.800 1.000 5 2001 2009
dbSNP: rs387906601
rs387906601
CYP11A1
1 1.000 15 74343953 missense variant A/G snv 0.800 1.000 5 2001 2009
dbSNP: rs72547508
rs72547508
CYP11A1
1 1.000 15 74339687 missense variant G/A snv 1.2E-05 7.0E-06 0.800 0
dbSNP: rs1567053134
rs1567053134
CYP11A1
8 0.925 0.040 15 74345160 frameshift variant AG/- del 0.700 0
dbSNP: rs886041121
rs886041121
CYP11A1
1 1.000 15 74342999 missense variant A/T snv 0.700 0