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: rs491567
rs491567
4 1.000 0.080 15 53654396 intron variant A/C snv 0.34 0.700 1.000 2 2010 2016
dbSNP: rs10518732
rs10518732
2 15 53646845 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10518733
rs10518733
1 15 53648110 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs35258188
rs35258188
4 1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 0.700 1.000 1 2018 2018