rs371513959

Orientation

plus

Stabilized

plus

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

Make rs371513959(A;A)

Make rs371513959(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43604384

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs371513959
dbSNP (classic)	rs371513959
ClinGen	rs371513959
ebi	rs371513959
HLI	rs371513959
Exac	rs371513959
Gnomad	rs371513959
Varsome	rs371513959
LitVar	rs371513959
Map	rs371513959
PheGenI	rs371513959
Biobank	rs371513959
1000 genomes	rs371513959
hgdp	rs371513959
ensembl	rs371513959
geneview	rs371513959
scholar	rs371513959
google	rs371513959
pharmgkb	rs371513959
gwascentral	rs371513959
openSNP	rs371513959
23andMe	rs371513959
SNPshot	rs371513959
SNPdbe	rs371513959
MSV3d	rs371513959
GWAS Ctlg	rs371513959

Max Magnitude

0

ClinVar
Risk	rs371513959(A;A)
Alt	rs371513959(A;A)
Reference	Rs371513959(C;C)
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.43896582C>A
CLNSRC
CLNACC	RCV000151949.1,