Variant #0007721024 (NC_000012.11:g.87381C>A)

Chromosome	12
Affects function (as reported)	Not classified
Affects function (by curator)	Not classified
DNA change (genomic) (Relative to hg19 / GRCh37)	g.87381C>A
DB-ID	-
dbSNP ID	rs782208329
gnomAD frequency	17/109866
gnomAD homozygote count	1/54917
Average frequency (gnomAD v.2.1.1)	Retrieve
Database submission license	No license selected
Created by	LOVD
Date created	2017-02-27 00:00:00 +01:00 (CET)
Date last edited	N/A

GnomAD v.2.1.1 dataset - Leiden Open Variation Database (LOVD)