rs181949335

Orientation

plus

Stabilized

plus

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

Make rs181949335(C;T)

Make rs181949335(T;T)

Reference

GRCh38 38.1/141

Chromosome

21

Position

42382101

Gene

TMPRSS3

is a	snp
is	mentioned by
dbSNP	rs181949335
dbSNP (classic)	rs181949335
ClinGen	rs181949335
ebi	rs181949335
HLI	rs181949335
Exac	rs181949335
Gnomad	rs181949335
Varsome	rs181949335
LitVar	rs181949335
Map	rs181949335
PheGenI	rs181949335
Biobank	rs181949335
1000 genomes	rs181949335
hgdp	rs181949335
ensembl	rs181949335
geneview	rs181949335
scholar	rs181949335
google	rs181949335
pharmgkb	rs181949335
gwascentral	rs181949335
openSNP	rs181949335
23andMe	rs181949335
SNPshot	rs181949335
SNPdbe	rs181949335
MSV3d	rs181949335
GWAS Ctlg	rs181949335

Max Magnitude

0

ClinVar
Risk	rs181949335(T;T)
Alt	rs181949335(T;T)
Reference	Rs181949335(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	TMPRSS3
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000021.8:g.43802210C>T
CLNSRC	ClinVar
CLNACC	RCV000039368.2,