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: rs4888378
rs4888378
1 0.851 0.040 16 75298143 intron variant A/G snv 0.52 0.720 1.000 1 2012 2018
dbSNP: rs12930452
rs12930452
1 1.000 0.040 16 75428157 intron variant A/G snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs3851738
rs3851738
1 1.000 0.040 16 75353635 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs8046696
rs8046696
1 1.000 0.040 16 75408245 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs8046697
rs8046697
2 0.925 0.080 16 75408246 intron variant T/C snv 0.51 0.700 1.000 1 2019 2019