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: rs769452
rs769452
2 0.925 0.160 19 44907853 missense variant T/C snv 2.5E-03 1.9E-03 0.700 1.000 3 2013 2016
dbSNP: rs769455
rs769455
8 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.700 1.000 3 2013 2016
dbSNP: rs267606664
rs267606664
5 0.851 0.120 19 44908730 missense variant G/A;C snv 1.6E-04; 6.3E-06 0.700 0
dbSNP: rs11542041
rs11542041
23 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2014 2014
dbSNP: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.010 1.000 1 2018 2018
dbSNP: rs7412
rs7412
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.010 1.000 1 2018 2018