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: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.100 0.944 18 2006 2019
dbSNP: rs769540300
rs769540300
8 0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 0.020 1.000 2 2008 2018
dbSNP: rs1187761291
rs1187761291
1 1.000 0.120 6 154039569 missense variant A/G snv 4.1E-06 0.010 < 0.001 1 2010 2010
dbSNP: rs200811844
rs200811844
1 1.000 0.120 6 154091110 missense variant T/C snv 1.8E-04 7.8E-04 0.010 1.000 1 2016 2016