rs876657725

Orientation

minus

Stabilized

minus

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

Make rs876657725(C;T)

Make rs876657725(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

43611237

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs876657725
dbSNP (classic)	rs876657725
ClinGen	rs876657725
ebi	rs876657725
HLI	rs876657725
Exac	rs876657725
Gnomad	rs876657725
Varsome	rs876657725
LitVar	rs876657725
Map	rs876657725
PheGenI	rs876657725
Biobank	rs876657725
1000 genomes	rs876657725
hgdp	rs876657725
ensembl	rs876657725
geneview	rs876657725
scholar	rs876657725
google	rs876657725
pharmgkb	rs876657725
gwascentral	rs876657725
openSNP	rs876657725
23andMe	rs876657725
SNPshot	rs876657725
SNPdbe	rs876657725
MSV3d	rs876657725
GWAS Ctlg	rs876657725

Max Magnitude

0

ClinVar
Risk	rs876657725(T;T)
Alt	rs876657725(T;T)
Reference	Rs876657725(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.43903435G>A
CLNSRC
CLNACC	RCV000218786.1,