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: rs121434427
rs121434427
2 0.923 0.036 1 161209912 missense variant G/A snp 0.700 1 2001 2001
dbSNP: rs121434428
rs121434428
2 0.923 0.036 1 161209915 missense variant C/A snp 0.700 1 2001 2001
dbSNP: rs121434429
rs121434429
2 0.923 0.036 1 161213673 missense variant T/C snp 0.700 1 2001 2001