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: rs17886395
rs17886395
2 0.925 0.120 10 79558907 missense variant C/G snv 0.19 0.16 0.010 1.000 1 2003 2003