rs121909062

Orientation

plus

Stabilized

plus

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

Make rs121909062(A;A)

Make rs121909062(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121187894

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909062
dbSNP (classic)	rs121909062
ClinGen	rs121909062
ebi	rs121909062
HLI	rs121909062
Exac	rs121909062
Gnomad	rs121909062
Varsome	rs121909062
LitVar	rs121909062
Map	rs121909062
PheGenI	rs121909062
Biobank	rs121909062
1000 genomes	rs121909062
hgdp	rs121909062
ensembl	rs121909062
geneview	rs121909062
scholar	rs121909062
google	rs121909062
pharmgkb	rs121909062
gwascentral	rs121909062
openSNP	rs121909062
23andMe	rs121909062
SNPshot	rs121909062
SNPdbe	rs121909062
MSV3d	rs121909062
GWAS Ctlg	rs121909062

Max Magnitude

0

OMIM	602574
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121909062(A;A)
Alt	rs121909062(A;A)
Reference	Rs121909062(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121058603G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007436.2,