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: rs3204689
rs3204689
1 1.000 0.040 15 57954604 3 prime UTR variant G/C snv 0.37 0.700 1.000 1 2014 2014
dbSNP: rs12915901
rs12915901
1 1.000 0.040 15 57987234 intron variant G/A snv 0.37 0.010 1.000 1 2018 2018
dbSNP: rs4238326
rs4238326
2 0.925 0.040 15 58043802 intron variant T/C snv 0.28 0.010 1.000 1 2017 2017