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: rs121909665
rs121909665
FSHR
2 0.925 0.160 2 48990629 missense variant G/T snv 0.810 1.000 8 2003 2018