rs121908355

Orientation

plus

Stabilized

plus

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

Make rs121908355(A;A)

Make rs121908355(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

71615573

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs121908355
dbSNP (classic)	rs121908355
ClinGen	rs121908355
ebi	rs121908355
HLI	rs121908355
Exac	rs121908355
Gnomad	rs121908355
Varsome	rs121908355
LitVar	rs121908355
Map	rs121908355
PheGenI	rs121908355
Biobank	rs121908355
1000 genomes	rs121908355
hgdp	rs121908355
ensembl	rs121908355
geneview	rs121908355
scholar	rs121908355
google	rs121908355
pharmgkb	rs121908355
gwascentral	rs121908355
openSNP	rs121908355
23andMe	rs121908355
SNPshot	rs121908355
SNPdbe	rs121908355
MSV3d	rs121908355
GWAS Ctlg	rs121908355

Max Magnitude

0

OMIM	605516
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121908355(A;A)
Alt	rs121908355(A;A)
Reference	Rs121908355(G;G)
Significance	Pathogenic
Disease	Deafness not specified
Variation	info
Gene	CDH23
CLNDBN	Deafness, autosomal recessive 12 not specified
Reversed	0
HGVS	NC_000010.10:g.73375330G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005212.3, RCV000173892.2,