rs876657726

Orientation

minus

Stabilized

minus

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

Make rs876657726(C;T)

Make rs876657726(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

43610317

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs876657726
dbSNP (classic)	rs876657726
ClinGen	rs876657726
ebi	rs876657726
HLI	rs876657726
Exac	rs876657726
Gnomad	rs876657726
Varsome	rs876657726
LitVar	rs876657726
Map	rs876657726
PheGenI	rs876657726
Biobank	rs876657726
1000 genomes	rs876657726
hgdp	rs876657726
ensembl	rs876657726
geneview	rs876657726
scholar	rs876657726
google	rs876657726
pharmgkb	rs876657726
gwascentral	rs876657726
openSNP	rs876657726
23andMe	rs876657726
SNPshot	rs876657726
SNPdbe	rs876657726
MSV3d	rs876657726
GWAS Ctlg	rs876657726

Max Magnitude

0

ClinVar
Risk	rs876657726(T;T)
Alt	rs876657726(T;T)
Reference	Rs876657726(C;C)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	STRC
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000015.9:g.43902515G>A
CLNSRC
CLNACC	RCV000222381.1,