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: rs104894118
rs104894118
NR5A1
4 0.882 0.080 9 124500196 missense variant C/A;T snv 1.6E-05; 4.1E-06 0.700 0
dbSNP: rs104894119
rs104894119
NR5A1
7 0.807 0.160 9 124500685 missense variant C/T snv 0.700 0