rs121908351

Orientation

plus

Stabilized

plus

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

Make rs121908351(A;A)

Make rs121908351(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

71732292

Gene	CDH23, C10orf105

is a	snp
is	mentioned by
dbSNP	rs121908351
dbSNP (classic)	rs121908351
ClinGen	rs121908351
ebi	rs121908351
HLI	rs121908351
Exac	rs121908351
Gnomad	rs121908351
Varsome	rs121908351
LitVar	rs121908351
Map	rs121908351
PheGenI	rs121908351
Biobank	rs121908351
1000 genomes	rs121908351
hgdp	rs121908351
ensembl	rs121908351
geneview	rs121908351
scholar	rs121908351
google	rs121908351
pharmgkb	rs121908351
gwascentral	rs121908351
openSNP	rs121908351
23andMe	rs121908351
SNPshot	rs121908351
SNPdbe	rs121908351
MSV3d	rs121908351
GWAS Ctlg	rs121908351

Max Magnitude

0

OMIM	605516
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121908351(A;A)
Alt	rs121908351(A;A)
Reference	Rs121908351(G;G)
Significance	Pathogenic
Disease	Deafness not provided
Variation	info
Gene	C10orf105 CDH23
CLNDBN	Deafness, autosomal recessive 12 not provided
Reversed	0
HGVS	NC_000010.10:g.73492049G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005205.4, RCV000436619.1,