rs727503443

Orientation

minus

Stabilized

minus

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

Make rs727503443(C;C)

Make rs727503443(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

43603362

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs727503443
dbSNP (classic)	rs727503443
ClinGen	rs727503443
ebi	rs727503443
HLI	rs727503443
Exac	rs727503443
Gnomad	rs727503443
Varsome	rs727503443
LitVar	rs727503443
Map	rs727503443
PheGenI	rs727503443
Biobank	rs727503443
1000 genomes	rs727503443
hgdp	rs727503443
ensembl	rs727503443
geneview	rs727503443
scholar	rs727503443
google	rs727503443
pharmgkb	rs727503443
gwascentral	rs727503443
openSNP	rs727503443
23andMe	rs727503443
SNPshot	rs727503443
SNPdbe	rs727503443
MSV3d	rs727503443
GWAS Ctlg	rs727503443

Max Magnitude

0

ClinVar
Risk	rs727503443(C;C)
Alt	rs727503443(C;C)
Reference	Rs727503443(G;G)
Significance	Probable-Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	STRC
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000015.9:g.43895560C>G
CLNSRC
CLNACC	RCV000151947.2,