rs121909061

Orientation

plus

Stabilized

plus

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

Make rs121909061(G;G)

Make rs121909061(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121166703

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909061
dbSNP (classic)	rs121909061
ClinGen	rs121909061
ebi	rs121909061
HLI	rs121909061
Exac	rs121909061
Gnomad	rs121909061
Varsome	rs121909061
LitVar	rs121909061
Map	rs121909061
PheGenI	rs121909061
Biobank	rs121909061
1000 genomes	rs121909061
hgdp	rs121909061
ensembl	rs121909061
geneview	rs121909061
scholar	rs121909061
google	rs121909061
pharmgkb	rs121909061
gwascentral	rs121909061
openSNP	rs121909061
23andMe	rs121909061
SNPshot	rs121909061
SNPdbe	rs121909061
MSV3d	rs121909061
GWAS Ctlg	rs121909061

Merged from

Rs121909064

Max Magnitude

0

OMIM	602574
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121909061(C;C) rs121909061(G;G)
Alt	rs121909061(C;C) rs121909061(G;G)
Reference	Rs121909061(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121037412T>C; NC_000011.9:g.121037412T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007438.2, RCV000007435.2,