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: rs11061946
rs11061946
2 1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs11061973
rs11061973
2 1.000 0.080 12 1756770 intron variant G/A snv 0.12 0.010 1.000 1 2011 2011