rs727503444

Orientation

minus

Stabilized

minus

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

Make rs727503444(C;T)

Make rs727503444(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

43608091

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs727503444
dbSNP (classic)	rs727503444
ClinGen	rs727503444
ebi	rs727503444
HLI	rs727503444
Exac	rs727503444
Gnomad	rs727503444
Varsome	rs727503444
LitVar	rs727503444
Map	rs727503444
PheGenI	rs727503444
Biobank	rs727503444
1000 genomes	rs727503444
hgdp	rs727503444
ensembl	rs727503444
geneview	rs727503444
scholar	rs727503444
google	rs727503444
pharmgkb	rs727503444
gwascentral	rs727503444
openSNP	rs727503444
23andMe	rs727503444
SNPshot	rs727503444
SNPdbe	rs727503444
MSV3d	rs727503444
GWAS Ctlg	rs727503444

Max Magnitude

0

ClinVar
Risk	rs727503444(T;T)
Alt	rs727503444(T;T)
Reference	Rs727503444(C;C)
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.43900289G>A
CLNSRC
CLNACC	RCV000151954.2,