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: rs121909051
rs121909051
1 1.000 0.080 3 167789273 missense variant T/C snv 0.800 1.000 2 1999 2002
dbSNP: rs121909052
rs121909052
1 1.000 0.080 3 167823019 missense variant A/G snv 0.700 0
dbSNP: rs121909053
rs121909053
3 0.882 0.120 3 167825265 missense variant G/A snv 0.700 0
dbSNP: rs121909054
rs121909054
1 1.000 0.080 3 167825264 missense variant G/A snv 0.700 0