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: rs588136
rs588136
5 15 58438299 intron variant C/G;T snv 0.800 1.000 2 2012 2017
dbSNP: rs7350789
rs7350789
4 15 58387469 intron variant G/A snv 0.35 0.700 1.000 2 2018 2019
dbSNP: rs8033940
rs8033940
5 15 58432643 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs8034802
rs8034802
5 15 58432593 intron variant T/A snv 0.33 0.700 1.000 1 2012 2012