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
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.100 0.909 11 2002 2014
dbSNP: rs375752214
rs375752214
13 0.756 0.214 7 150998541 missense variant C/T snp 4.1E-06 3.2E-05 0.010 1.000 1 2004 2004
dbSNP: rs743507
rs743507
3 0.923 0.143 7 151010400 intron variant C/T snp 0.78 0.010 1.000 1 2010 2010