rs121909059

Orientation

plus

Stabilized

plus

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

Make rs121909059(A;A)

Make rs121909059(A;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121137648

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909059
dbSNP (classic)	rs121909059
ClinGen	rs121909059
ebi	rs121909059
HLI	rs121909059
Exac	rs121909059
Gnomad	rs121909059
Varsome	rs121909059
LitVar	rs121909059
Map	rs121909059
PheGenI	rs121909059
Biobank	rs121909059
1000 genomes	rs121909059
hgdp	rs121909059
ensembl	rs121909059
geneview	rs121909059
scholar	rs121909059
google	rs121909059
pharmgkb	rs121909059
gwascentral	rs121909059
openSNP	rs121909059
23andMe	rs121909059
SNPshot	rs121909059
SNPdbe	rs121909059
MSV3d	rs121909059
GWAS Ctlg	rs121909059

Max Magnitude

0

OMIM	602574
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909059(A;A)
Alt	rs121909059(A;A)
Reference	Rs121909059(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121008357T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007431.2,