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: rs1554770620
rs1554770620
1 1.000 0.080 9 128633958 missense variant T/G snv 0.700 0
dbSNP: rs1554771066
rs1554771066
1 1.000 0.080 9 128634843 missense variant T/C snv 0.700 0