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: rs1555303073
rs1555303073
6 0.851 0.120 13 110176912 missense variant C/T snv 0.700 1.000 1 2013 2013
dbSNP: rs587777379
rs587777379
1 1.000 0.080 13 110166277 missense variant C/T snv 0.700 1.000 1 2013 2013