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: rs17293632
rs17293632
12 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.800 1.000 3 2012 2017
dbSNP: rs36221701
rs36221701
1 15 67064151 non coding transcript exon variant T/C;G snv 0.010 1.000 1 2018 2018