rs727505074

Orientation

minus

Stabilized

minus

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

Make rs727505074(-;-)

Make rs727505074(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43610326

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs727505074
dbSNP (classic)	rs727505074
ClinGen	rs727505074
ebi	rs727505074
HLI	rs727505074
Exac	rs727505074
Gnomad	rs727505074
Varsome	rs727505074
LitVar	rs727505074
Map	rs727505074
PheGenI	rs727505074
Biobank	rs727505074
1000 genomes	rs727505074
hgdp	rs727505074
ensembl	rs727505074
geneview	rs727505074
scholar	rs727505074
google	rs727505074
pharmgkb	rs727505074
gwascentral	rs727505074
openSNP	rs727505074
23andMe	rs727505074
SNPshot	rs727505074
SNPdbe	rs727505074
MSV3d	rs727505074
GWAS Ctlg	rs727505074

Max Magnitude

0

ClinVar
Risk	rs727505074(-;-)
Alt	rs727505074(-;-)
Reference	Rs727505074(T;T)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	STRC
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	1
HGVS	NC_000015.9:g.43902524delA
CLNSRC
CLNACC	RCV000156514.1,