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: rs1057517858
rs1057517858
3 0.925 0.240 12 49185714 missense variant C/A;T snv 0.700 0
dbSNP: rs1064796460
rs1064796460
8 0.790 0.400 12 49185197 missense variant C/G;T snv 0.700 0
dbSNP: rs1565627707
rs1565627707
3 0.925 0.240 12 49186657 missense variant C/A snv 0.700 0
dbSNP: rs797045005
rs797045005
4 0.851 0.320 12 49185140 missense variant A/G snv 0.700 0