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: rs1378379005
rs1378379005
1 19 12938723 missense variant C/G;T snv 2.1E-05 0.010 1.000 1 2016 2016
dbSNP: rs147368353
rs147368353
1 19 12938729 missense variant C/G;T snv 6.3E-05; 5.8E-05 0.010 1.000 1 2016 2016