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: rs1057519320
rs1057519320
7 0.807 0.160 15 48444574 missense variant G/A snv 0.700 0
dbSNP: rs1057519321
rs1057519321
7 0.807 0.160 5 128349391 missense variant C/A;T snv 0.700 0
dbSNP: rs1566528711
rs1566528711
6 0.851 0.240 13 20189338 missense variant T/C snv 0.700 0