rs876657728

Orientation

plus

Stabilized

plus

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

Make rs876657728(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

72805491

Gene

TMC1

is a	snp
is	mentioned by
dbSNP	rs876657728
dbSNP (classic)	rs876657728
ClinGen	rs876657728
ebi	rs876657728
HLI	rs876657728
Exac	rs876657728
Gnomad	rs876657728
Varsome	rs876657728
LitVar	rs876657728
Map	rs876657728
PheGenI	rs876657728
Biobank	rs876657728
1000 genomes	rs876657728
hgdp	rs876657728
ensembl	rs876657728
geneview	rs876657728
scholar	rs876657728
google	rs876657728
pharmgkb	rs876657728
gwascentral	rs876657728
openSNP	rs876657728
23andMe	rs876657728
SNPshot	rs876657728
SNPdbe	rs876657728
MSV3d	rs876657728
GWAS Ctlg	rs876657728

Max Magnitude

3

ClinVar
Risk	rs876657728(A;A)
Alt	rs876657728(A;A)
Reference	Rs876657728(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	TMC1
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000009.11:g.75420407G>A
CLNSRC
CLNACC	RCV000219905.1,