rs876657727

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;T)	3	Carrier of a DFNB7/11 deafness mutation
(T;T)	0	common in clinvar

Make rs876657727(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

72791897

Gene

TMC1

is a	snp
is	mentioned by
dbSNP	rs876657727
dbSNP (classic)	rs876657727
ClinGen	rs876657727
ebi	rs876657727
HLI	rs876657727
Exac	rs876657727
Gnomad	rs876657727
Varsome	rs876657727
LitVar	rs876657727
Map	rs876657727
PheGenI	rs876657727
Biobank	rs876657727
1000 genomes	rs876657727
hgdp	rs876657727
ensembl	rs876657727
geneview	rs876657727
scholar	rs876657727
google	rs876657727
pharmgkb	rs876657727
gwascentral	rs876657727
openSNP	rs876657727
23andMe	rs876657727
SNPshot	rs876657727
SNPdbe	rs876657727
MSV3d	rs876657727
GWAS Ctlg	rs876657727

Max Magnitude

3

ClinVar
Risk	rs876657727(-;-)
Alt	rs876657727(-;-)
Reference	Rs876657727(T;T)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness not provided
Variation	info
Gene	TMC1
CLNDBN	Nonsyndromic hearing loss and deafness not provided
Reversed	0
HGVS	NC_000009.11:g.75406813delT
CLNSRC
CLNACC	RCV000217598.1, RCV000413125.1,