rs139956283

Orientation

plus

Stabilized

plus

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

Make rs139956283(A;A)

Make rs139956283(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43600011

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs139956283
dbSNP (classic)	rs139956283
ClinGen	rs139956283
ebi	rs139956283
HLI	rs139956283
Exac	rs139956283
Gnomad	rs139956283
Varsome	rs139956283
LitVar	rs139956283
Map	rs139956283
PheGenI	rs139956283
Biobank	rs139956283
1000 genomes	rs139956283
hgdp	rs139956283
ensembl	rs139956283
geneview	rs139956283
scholar	rs139956283
google	rs139956283
pharmgkb	rs139956283
gwascentral	rs139956283
openSNP	rs139956283
23andMe	rs139956283
SNPshot	rs139956283
SNPdbe	rs139956283
MSV3d	rs139956283
GWAS Ctlg	rs139956283

Max Magnitude

0

ClinVar
Risk	rs139956283(A;A)
Alt	rs139956283(A;A)
Reference	Rs139956283(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.43892209G>A
CLNSRC
CLNACC	RCV000151937.1,