Variant #0009515986 (NC_000016.9:g.65541T>G)

Chromosome	16
Affects function (as reported)	Not classified
Affects function (by curator)	Not classified
DNA change (genomic) (Relative to hg19 / GRCh37)	g.65541T>G
DB-ID	-
dbSNP ID	-
gnomAD frequency	2/42836
gnomAD homozygote count	1/21417
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)