rs377480477

Orientation

plus

Stabilized

plus

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

Make rs377480477(A;A)

Make rs377480477(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43603385

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs377480477
dbSNP (classic)	rs377480477
ClinGen	rs377480477
ebi	rs377480477
HLI	rs377480477
Exac	rs377480477
Gnomad	rs377480477
Varsome	rs377480477
LitVar	rs377480477
Map	rs377480477
PheGenI	rs377480477
Biobank	rs377480477
1000 genomes	rs377480477
hgdp	rs377480477
ensembl	rs377480477
geneview	rs377480477
scholar	rs377480477
google	rs377480477
pharmgkb	rs377480477
gwascentral	rs377480477
openSNP	rs377480477
23andMe	rs377480477
SNPshot	rs377480477
SNPdbe	rs377480477
MSV3d	rs377480477
GWAS Ctlg	rs377480477

Max Magnitude

0

ClinVar
Risk	rs377480477(A;A)
Alt	rs377480477(A;A)
Reference	Rs377480477(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	STRC
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000015.9:g.43895583G>A
CLNSRC
CLNACC	RCV000156556.2,