rs121909058

Orientation

plus

Stabilized

plus

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

Make rs121909058(A;G)

Make rs121909058(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121168076

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909058
dbSNP (classic)	rs121909058
ClinGen	rs121909058
ebi	rs121909058
HLI	rs121909058
Exac	rs121909058
Gnomad	rs121909058
Varsome	rs121909058
LitVar	rs121909058
Map	rs121909058
PheGenI	rs121909058
Biobank	rs121909058
1000 genomes	rs121909058
hgdp	rs121909058
ensembl	rs121909058
geneview	rs121909058
scholar	rs121909058
google	rs121909058
pharmgkb	rs121909058
gwascentral	rs121909058
openSNP	rs121909058
23andMe	rs121909058
SNPshot	rs121909058
SNPdbe	rs121909058
MSV3d	rs121909058
GWAS Ctlg	rs121909058

Merged from

Rs28939690

Max Magnitude

0

OMIM	602574
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909058(G;G)
Alt	rs121909058(G;G)
Reference	Rs121909058(A;A)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121038785A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007429.2,