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: rs11627485
rs11627485
5 14 65020976 intron variant T/C snv 0.36 0.700 1.000 2 2016 2019
dbSNP: rs7155454
rs7155454
4 14 65035521 intron variant G/A snv 0.61 0.700 1.000 2 2012 2017