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: rs3760213
rs3760213
SHBG
1 1.000 0.040 17 7629896 intron variant G/A snv 7.8E-02 0.010 1.000 1 2014 2014