rs397515435

Orientation

minus

Stabilized

minus

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

Make rs397515435(A;A)

Make rs397515435(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26480968

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515435
dbSNP (classic)	rs397515435
ClinGen	rs397515435
ebi	rs397515435
HLI	rs397515435
Exac	rs397515435
Gnomad	rs397515435
Varsome	rs397515435
LitVar	rs397515435
Map	rs397515435
PheGenI	rs397515435
Biobank	rs397515435
1000 genomes	rs397515435
hgdp	rs397515435
ensembl	rs397515435
geneview	rs397515435
scholar	rs397515435
google	rs397515435
pharmgkb	rs397515435
gwascentral	rs397515435
openSNP	rs397515435
23andMe	rs397515435
SNPshot	rs397515435
SNPdbe	rs397515435
MSV3d	rs397515435
GWAS Ctlg	rs397515435

Max Magnitude

0

ClinVar
Risk	rs397515435(A;A)
Alt	rs397515435(A;A)
Reference	Rs397515435(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26703836C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000033199.2,