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: rs10093547
rs10093547
3 0.882 0.040 8 76562310 intron variant T/G snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs28727938
rs28727938
3 0.882 0.040 8 76566304 intron variant C/G snv 1.0E-01 0.700 1.000 1 2015 2015
dbSNP: rs35251485
rs35251485
3 0.882 0.040 8 76571195 intron variant G/A snv 1.0E-01 0.700 1.000 1 2019 2019