rs397515606

Orientation

minus

Stabilized

minus

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

Make rs397515606(G;G)

Make rs397515606(G;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

26461845

Gene

OTOF

is a	snp
is	mentioned by
dbSNP	rs397515606
dbSNP (classic)	rs397515606
ClinGen	rs397515606
ebi	rs397515606
HLI	rs397515606
Exac	rs397515606
Gnomad	rs397515606
Varsome	rs397515606
LitVar	rs397515606
Map	rs397515606
PheGenI	rs397515606
Biobank	rs397515606
1000 genomes	rs397515606
hgdp	rs397515606
ensembl	rs397515606
geneview	rs397515606
scholar	rs397515606
google	rs397515606
pharmgkb	rs397515606
gwascentral	rs397515606
openSNP	rs397515606
23andMe	rs397515606
SNPshot	rs397515606
SNPdbe	rs397515606
MSV3d	rs397515606
GWAS Ctlg	rs397515606

Max Magnitude

0

ClinVar
Risk	rs397515606(G;G)
Alt	rs397515606(G;G)
Reference	Rs397515606(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	OTOF
CLNDBN	Deafness, autosomal recessive 9
Reversed	1
HGVS	NC_000002.11:g.26684713A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000056049.1,