rs876657724

Orientation

minus

Stabilized

minus

Make rs876657724(A;A)

Make rs876657724(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

43616480

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs876657724
dbSNP (classic)	rs876657724
ClinGen	rs876657724
ebi	rs876657724
HLI	rs876657724
Exac	rs876657724
Gnomad	rs876657724
Varsome	rs876657724
LitVar	rs876657724
Map	rs876657724
PheGenI	rs876657724
Biobank	rs876657724
1000 genomes	rs876657724
hgdp	rs876657724
ensembl	rs876657724
geneview	rs876657724
scholar	rs876657724
google	rs876657724
pharmgkb	rs876657724
gwascentral	rs876657724
openSNP	rs876657724
23andMe	rs876657724
SNPshot	rs876657724
SNPdbe	rs876657724
MSV3d	rs876657724
GWAS Ctlg	rs876657724

Max Magnitude

0

ClinVar
Risk	rs876657724(A;A)
Alt	rs876657724(A;A)
Reference	Rs876657724(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.43908678G>T
CLNSRC
CLNACC	RCV000215137.1,