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: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.100 0.895 19 2002 2020
dbSNP: rs1341139296
rs1341139296
1 7 150998546 missense variant A/G snv 8.2E-06 0.010 1.000 1 2017 2017
dbSNP: rs375752214
rs375752214
22 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 0.010 1.000 1 2004 2004
dbSNP: rs3918226
rs3918226
12 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs743507
rs743507
4 0.882 0.200 7 151010400 intron variant C/T snv 0.77 0.010 1.000 1 2010 2010