rs121909060

Orientation

plus

Stabilized

plus

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

Make rs121909060(C;C)

Make rs121909060(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121160301

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909060
dbSNP (classic)	rs121909060
ClinGen	rs121909060
ebi	rs121909060
HLI	rs121909060
Exac	rs121909060
Gnomad	rs121909060
Varsome	rs121909060
LitVar	rs121909060
Map	rs121909060
PheGenI	rs121909060
Biobank	rs121909060
1000 genomes	rs121909060
hgdp	rs121909060
ensembl	rs121909060
geneview	rs121909060
scholar	rs121909060
google	rs121909060
pharmgkb	rs121909060
gwascentral	rs121909060
openSNP	rs121909060
23andMe	rs121909060
SNPshot	rs121909060
SNPdbe	rs121909060
MSV3d	rs121909060
GWAS Ctlg	rs121909060

Merged from

Rs28939691

Max Magnitude

0

OMIM	602574
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909060(C;C)
Alt	rs121909060(C;C)
Reference	Rs121909060(G;G)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121031010G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007432.2,