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: rs76863441
rs76863441
25 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 0.760 0.714 7 2009 2017
dbSNP: rs1051931
rs1051931
19 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 0.040 0.250 4 2010 2018
dbSNP: rs1805017
rs1805017
5 0.851 0.240 6 46716485 missense variant C/A;T snv 4.0E-06; 0.31 0.040 1.000 4 2010 2018
dbSNP: rs1805018
rs1805018
6 0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 0.040 0.750 4 2009 2018
dbSNP: rs16874954
rs16874954
2 0.925 0.040 6 46709361 missense variant C/A snv 0.010 < 0.001 1 2018 2018
dbSNP: rs9395208
rs9395208
1 1.000 0.040 6 46735582 5 prime UTR variant G/C snv 0.20 0.010 1.000 1 2016 2016