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: rs1538979
rs1538979
3 0.882 0.160 1 231761122 intron variant C/T snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2011 2011
dbSNP: rs821577
rs821577
3 0.882 0.160 1 231931311 intron variant T/C;G snv 0.010 1.000 1 2009 2009
dbSNP: rs821633
rs821633
3 0.882 0.160 1 232013187 intron variant T/C snv 0.37 0.010 1.000 1 2009 2009