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 0.030 0.667 3 2011 2017
dbSNP: rs557748
rs557748
1 1.000 0.080 6 154043167 intron variant G/A snv 0.19 0.010 1.000 1 2014 2014
dbSNP: rs774507706
rs774507706
1 1.000 0.080 6 154091093 missense variant A/G snv 4.0E-06 0.010 1.000 1 2011 2011