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: rs1553196096
rs1553196096
5 1 22086463 missense variant G/A snv 0.700 0
dbSNP: rs1553196101
rs1553196101
8 0.925 0.080 1 22086507 missense variant T/C snv 0.700 0
dbSNP: rs1553196134
rs1553196134
6 0.925 0.080 1 22086856 missense variant C/T snv 0.700 0