rs876657661

Orientation

plus

Stabilized

plus

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

Make rs876657661(A;T)

Make rs876657661(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

121189078

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs876657661
dbSNP (classic)	rs876657661
ClinGen	rs876657661
ebi	rs876657661
HLI	rs876657661
Exac	rs876657661
Gnomad	rs876657661
Varsome	rs876657661
LitVar	rs876657661
Map	rs876657661
PheGenI	rs876657661
Biobank	rs876657661
1000 genomes	rs876657661
hgdp	rs876657661
ensembl	rs876657661
geneview	rs876657661
scholar	rs876657661
google	rs876657661
pharmgkb	rs876657661
gwascentral	rs876657661
openSNP	rs876657661
23andMe	rs876657661
SNPshot	rs876657661
SNPdbe	rs876657661
MSV3d	rs876657661
GWAS Ctlg	rs876657661

Max Magnitude

0

ClinVar
Risk	rs876657661(T;T)
Alt	rs876657661(T;T)
Reference	Rs876657661(A;A)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	TECTA
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000011.9:g.121059787A>T
CLNSRC
CLNACC	RCV000214219.1,