rs730880359

Orientation

plus

Stabilized

plus

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

Make rs730880359(GGAGG;GGAGG)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

72694697

Gene

TMC1

is a	snp
is	mentioned by
dbSNP	rs730880359
dbSNP (classic)	rs730880359
ClinGen	rs730880359
ebi	rs730880359
HLI	rs730880359
Exac	rs730880359
Gnomad	rs730880359
Varsome	rs730880359
LitVar	rs730880359
Map	rs730880359
PheGenI	rs730880359
Biobank	rs730880359
1000 genomes	rs730880359
hgdp	rs730880359
ensembl	rs730880359
geneview	rs730880359
scholar	rs730880359
google	rs730880359
pharmgkb	rs730880359
gwascentral	rs730880359
openSNP	rs730880359
23andMe	rs730880359
SNPshot	rs730880359
SNPdbe	rs730880359
MSV3d	rs730880359
GWAS Ctlg	rs730880359

Max Magnitude

3

ClinVar
Risk	rs730880359(GGAGG;GGAGG)
Alt	rs730880359(GGAGG;GGAGG)
Reference	Rs730880359(-;-)
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.75309609_75309613dupGGAGG
CLNSRC
CLNACC	RCV000156220.1,