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: rs104894119
rs104894119
NR5A1
7 0.807 0.160 9 124500685 missense variant C/T snv 0.800 1.000 4 2016 2017
dbSNP: rs886039769
rs886039769
NR5A1
10 0.807 0.160 9 124500686 missense variant G/A snv 0.800 1.000 4 2016 2017