rs370088722

Orientation

plus

Stabilized

plus

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

Make rs370088722(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

72754817

Gene

TMC1

is a	snp
is	mentioned by
dbSNP	rs370088722
dbSNP (classic)	rs370088722
ClinGen	rs370088722
ebi	rs370088722
HLI	rs370088722
Exac	rs370088722
Gnomad	rs370088722
Varsome	rs370088722
LitVar	rs370088722
Map	rs370088722
PheGenI	rs370088722
Biobank	rs370088722
1000 genomes	rs370088722
hgdp	rs370088722
ensembl	rs370088722
geneview	rs370088722
scholar	rs370088722
google	rs370088722
pharmgkb	rs370088722
gwascentral	rs370088722
openSNP	rs370088722
23andMe	rs370088722
SNPshot	rs370088722
SNPdbe	rs370088722
MSV3d	rs370088722
GWAS Ctlg	rs370088722

Max Magnitude

0

ClinVar
Risk	rs370088722(T;T)
Alt	rs370088722(T;T)
Reference	Rs370088722(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness Deafness
Variation	info
Gene	TMC1
CLNDBN	Nonsyndromic hearing loss and deafness Deafness, autosomal recessive 7
Reversed	0
HGVS	NC_000009.11:g.75369733C>T
CLNSRC	ClinVar
CLNACC	RCV000041146.3, RCV000225031.1,