rs199839039

Orientation

plus

Stabilized

plus

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

Make rs199839039(C;T)

Make rs199839039(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43601395

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs199839039
dbSNP (classic)	rs199839039
ClinGen	rs199839039
ebi	rs199839039
HLI	rs199839039
Exac	rs199839039
Gnomad	rs199839039
Varsome	rs199839039
LitVar	rs199839039
Map	rs199839039
PheGenI	rs199839039
Biobank	rs199839039
1000 genomes	rs199839039
hgdp	rs199839039
ensembl	rs199839039
geneview	rs199839039
scholar	rs199839039
google	rs199839039
pharmgkb	rs199839039
gwascentral	rs199839039
openSNP	rs199839039
23andMe	rs199839039
SNPshot	rs199839039
SNPdbe	rs199839039
MSV3d	rs199839039
GWAS Ctlg	rs199839039

Max Magnitude

0

ClinVar
Risk	rs199839039(T;T)
Alt	rs199839039(T;T)
Reference	Rs199839039(C;C)
Significance	Pathogenic
Disease	Deafness Nonsyndromic hearing loss and deafness
Variation	info
Gene	STRC
CLNDBN	Deafness, autosomal recessive 16 Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000015.9:g.43893593C>T
CLNSRC
CLNACC	RCV000151944.4, RCV000211855.1,