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: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.710 1.000 1 1999 1999
dbSNP: rs1227507479
rs1227507479
1 1.000 0.160 6 26092783 missense variant T/C snv 4.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs28934595
rs28934595
2 0.925 0.160 6 26091354 missense variant A/C snv 0.010 1.000 1 1999 1999