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: rs11631591
rs11631591
1 1.000 0.080 15 38558061 intron variant T/C snv 0.41 0.010 1.000 1 2019 2019