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: rs6795735
rs6795735
7 0.882 0.120 3 64719689 intron variant C/A;G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs2371767
rs2371767
5 3 64732582 intron variant G/C snv 0.38 0.700 1.000 2 2018 2019
dbSNP: rs66815886
rs66815886
1 3 64717718 intron variant G/T snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs7372321
rs7372321
1 3 64728139 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs76699125
rs76699125
1 3 64715859 intron variant T/C snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs9860730
rs9860730
3 3 64715470 intron variant A/G snv 0.50 0.700 1.000 1 2015 2015