rs794729665

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs794729665(A;C)

Make rs794729665(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

24178385

Gene

DCDC2

is a	snp
is	mentioned by
dbSNP	rs794729665
dbSNP (classic)	rs794729665
ClinGen	rs794729665
ebi	rs794729665
HLI	rs794729665
Exac	rs794729665
Gnomad	rs794729665
Varsome	rs794729665
LitVar	rs794729665
Map	rs794729665
PheGenI	rs794729665
Biobank	rs794729665
1000 genomes	rs794729665
hgdp	rs794729665
ensembl	rs794729665
geneview	rs794729665
scholar	rs794729665
google	rs794729665
pharmgkb	rs794729665
gwascentral	rs794729665
openSNP	rs794729665
23andMe	rs794729665
SNPshot	rs794729665
SNPdbe	rs794729665
MSV3d	rs794729665
GWAS Ctlg	rs794729665

Max Magnitude

0

ClinVar
Risk	rs794729665(C;C)
Alt	rs794729665(C;C)
Reference	Rs794729665(A;A)
Significance	Pathogenic
Disease	Nonsyndromic Deafness Deafness
Variation	info
Gene	DCDC2
CLNDBN	Nonsyndromic Deafness Deafness, autosomal recessive 66
Reversed	1
HGVS	NC_000006.11:g.24178613T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000157618.2, RCV000185587.4,