Source: ALL
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: rs767159114
rs767159114
HGD
1 1.000 0.080 3 120628517 missense variant C/G snv 4.0E-06 0.800 1.000 14 1996 2016