rs786200882

Orientation

minus

Stabilized

minus

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

Make rs786200882(-;C)

Make rs786200882(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

43611297

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs786200882
dbSNP (classic)	rs786200882
ClinGen	rs786200882
ebi	rs786200882
HLI	rs786200882
Exac	rs786200882
Gnomad	rs786200882
Varsome	rs786200882
LitVar	rs786200882
Map	rs786200882
PheGenI	rs786200882
Biobank	rs786200882
1000 genomes	rs786200882
hgdp	rs786200882
ensembl	rs786200882
geneview	rs786200882
scholar	rs786200882
google	rs786200882
pharmgkb	rs786200882
gwascentral	rs786200882
openSNP	rs786200882
23andMe	rs786200882
SNPshot	rs786200882
SNPdbe	rs786200882
MSV3d	rs786200882
GWAS Ctlg	rs786200882

Max Magnitude

0

ClinVar
Risk	rs786200882(C;C)
Alt	rs786200882(C;C)
Reference	Rs786200882(-;-)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	STRC
CLNDBN	Deafness, autosomal recessive 16
Reversed	1
HGVS	NC_000015.9:g.43903496dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004591.3,