rs431905513

Orientation

minus

Stabilized

minus

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

Make rs431905513(A;T)

Make rs431905513(T;T)

Reference

GRCh38 38.1/142

Chromosome

9

Position

115040947

Gene

TNC

is a	snp
is	mentioned by
dbSNP	rs431905513
dbSNP (classic)	rs431905513
ClinGen	rs431905513
ebi	rs431905513
HLI	rs431905513
Exac	rs431905513
Gnomad	rs431905513
Varsome	rs431905513
LitVar	rs431905513
Map	rs431905513
PheGenI	rs431905513
Biobank	rs431905513
1000 genomes	rs431905513
hgdp	rs431905513
ensembl	rs431905513
geneview	rs431905513
scholar	rs431905513
google	rs431905513
pharmgkb	rs431905513
gwascentral	rs431905513
openSNP	rs431905513
23andMe	rs431905513
SNPshot	rs431905513
SNPdbe	rs431905513
MSV3d	rs431905513
GWAS Ctlg	rs431905513

Max Magnitude

0

ClinVar
Risk	rs431905513(T;T)
Alt	rs431905513(T;T)
Reference	Rs431905513(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TNC
CLNDBN	Deafness, autosomal dominant 56
Reversed	1
HGVS	NC_000009.11:g.117803226T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000083260.2,