rs774312182

Orientation

plus

Stabilized

plus

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

Make rs774312182(A;A)

Make rs774312182(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

43604720

Gene

STRC

is a	snp
is	mentioned by
dbSNP	rs774312182
dbSNP (classic)	rs774312182
ClinGen	rs774312182
ebi	rs774312182
HLI	rs774312182
Exac	rs774312182
Gnomad	rs774312182
Varsome	rs774312182
LitVar	rs774312182
Map	rs774312182
PheGenI	rs774312182
Biobank	rs774312182
1000 genomes	rs774312182
hgdp	rs774312182
ensembl	rs774312182
geneview	rs774312182
scholar	rs774312182
google	rs774312182
pharmgkb	rs774312182
gwascentral	rs774312182
openSNP	rs774312182
23andMe	rs774312182
SNPshot	rs774312182
SNPdbe	rs774312182
MSV3d	rs774312182
GWAS Ctlg	rs774312182

Max Magnitude

0

ClinVar
Risk	rs774312182(A;A)
Alt	rs774312182(A;A)
Reference	Rs774312182(G;G)
Significance	Pathogenic
Disease	Deafness not provided
Variation	info
Gene	STRC
CLNDBN	Deafness, autosomal dominant 16 not provided
Reversed	0
HGVS	NC_000015.9:g.43896918G>A
CLNSRC
CLNACC	RCV000225080.1, RCV000428482.1,