rs397514588

Orientation

plus

Stabilized

plus

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

Make rs397514588(C;T)

Make rs397514588(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

80229341

Gene

OTOGL

is a	snp
is	mentioned by
dbSNP	rs397514588
dbSNP (classic)	rs397514588
ClinGen	rs397514588
ebi	rs397514588
HLI	rs397514588
Exac	rs397514588
Gnomad	rs397514588
Varsome	rs397514588
LitVar	rs397514588
Map	rs397514588
PheGenI	rs397514588
Biobank	rs397514588
1000 genomes	rs397514588
hgdp	rs397514588
ensembl	rs397514588
geneview	rs397514588
scholar	rs397514588
google	rs397514588
pharmgkb	rs397514588
gwascentral	rs397514588
openSNP	rs397514588
23andMe	rs397514588
SNPshot	rs397514588
SNPdbe	rs397514588
MSV3d	rs397514588
GWAS Ctlg	rs397514588

Max Magnitude

0

ClinVar
Risk	rs397514588(T;T)
Alt	rs397514588(T;T)
Reference	Rs397514588(C;C)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOGL
CLNDBN	Deafness, autosomal recessive 84b
Reversed	0
HGVS	NC_000012.11:g.80623121C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033001.3,