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: rs1800450
rs1800450
26 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 0.030 0.667 3 2014 2019
dbSNP: rs1800451
rs1800451
9 0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 0.030 1.000 3 2011 2019
dbSNP: rs11003125
rs11003125
7 0.790 0.480 10 52772254 upstream gene variant G/C snv 0.31 0.020 0.500 2 2017 2019
dbSNP: rs5030737
rs5030737
11 0.752 0.360 10 52771482 missense variant G/A snv 5.6E-02 5.0E-02 0.020 1.000 2 2019 2019
dbSNP: rs7095891
rs7095891
3 0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 0.020 1.000 2 2019 2019
dbSNP: rs7096206
rs7096206
17 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 0.020 0.500 2 2014 2019