rs876657716

Orientation

plus

Stabilized

plus

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

Make rs876657716(A;A)

Make rs876657716(A;CTGCTT)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

21697781

Gene

OTOA

is a	snp
is	mentioned by
dbSNP	rs876657716
dbSNP (classic)	rs876657716
ClinGen	rs876657716
ebi	rs876657716
HLI	rs876657716
Exac	rs876657716
Gnomad	rs876657716
Varsome	rs876657716
LitVar	rs876657716
Map	rs876657716
PheGenI	rs876657716
Biobank	rs876657716
1000 genomes	rs876657716
hgdp	rs876657716
ensembl	rs876657716
geneview	rs876657716
scholar	rs876657716
google	rs876657716
pharmgkb	rs876657716
gwascentral	rs876657716
openSNP	rs876657716
23andMe	rs876657716
SNPshot	rs876657716
SNPdbe	rs876657716
MSV3d	rs876657716
GWAS Ctlg	rs876657716

Max Magnitude

0

ClinVar
Risk	rs876657716(A;A)
Alt	rs876657716(A;A)
Reference	Rs876657716(CTGCTT;CTGCTT)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOA
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000016.9:g.21709102_21709107delinsA
CLNSRC
CLNACC	RCV000222173.1,