Gene: SHBG ×
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: rs6259
rs6259
SHBG
27 0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 0.060 0.833 6 2003 2012
dbSNP: rs6257
rs6257
SHBG
5 0.827 0.200 17 7630399 3 prime UTR variant T/C snv 9.4E-02 8.1E-02 0.010 1.000 1 2008 2008