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: rs11575935
rs11575935
2 0.925 0.040 19 18063921 missense variant C/T snv 1.1E-02 5.7E-03 0.010 1.000 1 2007 2007