rs372526764

Orientation

plus

Stabilized

plus

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

Make rs372526764(C;T)

Make rs372526764(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

21

Position

42383088

Gene

TMPRSS3

is a	snp
is	mentioned by
dbSNP	rs372526764
dbSNP (classic)	rs372526764
ClinGen	rs372526764
ebi	rs372526764
HLI	rs372526764
Exac	rs372526764
Gnomad	rs372526764
Varsome	rs372526764
LitVar	rs372526764
Map	rs372526764
PheGenI	rs372526764
Biobank	rs372526764
1000 genomes	rs372526764
hgdp	rs372526764
ensembl	rs372526764
geneview	rs372526764
scholar	rs372526764
google	rs372526764
pharmgkb	rs372526764
gwascentral	rs372526764
openSNP	rs372526764
23andMe	rs372526764
SNPshot	rs372526764
SNPdbe	rs372526764
MSV3d	rs372526764
GWAS Ctlg	rs372526764

Max Magnitude

0

ClinVar
Risk	rs372526764(T;T)
Alt	rs372526764(T;T)
Reference	Rs372526764(C;C)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness Deafness
Variation	info
Gene	TMPRSS3
CLNDBN	Nonsyndromic hearing loss and deafness Deafness, autosomal recessive 8
Reversed	0
HGVS	NC_000021.8:g.43803197C>T
CLNSRC
CLNACC	RCV000155297.1, RCV000487440.1,