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: rs1323910952
rs1323910952
1 1.000 0.080 11 65546882 missense variant C/A snv 0.010 1.000 1 2019 2019
dbSNP: rs1554974135
rs1554974135
2 0.925 0.080 11 65547459 missense variant G/C snv 0.010 1.000 1 2016 2016