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: rs11770757
rs11770757
1 1.000 0.080 7 134063193 intron variant G/A;C snv 0.800 1.000 1 2014 2014