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: rs10749053
rs10749053
1 1.000 0.080 10 110816937 intron variant T/A;C snv 0.700 1.000 2 2018 2018
dbSNP: rs35141404
rs35141404
1 1.000 0.080 10 110644544 synonymous variant G/A snv 0.14 0.21 0.010 1.000 1 2012 2012