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 0.010 1.000 1 2013 2013
dbSNP: rs748409227
rs748409227
2 8 41708865 synonymous variant C/T snv 1.6E-05 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1800866
rs1800866
8 0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 0.010 1.000 1 2019 2019
dbSNP: rs4680
rs4680
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2020 2020