rs121909064

Merged into

rs121909061

Orientation

plus

Stabilized

plus

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

Make rs121909064(C;C)

Make rs121909064(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

121166703

Gene

TECTA

is a	snp
is	mentioned by
dbSNP	rs121909064
dbSNP (classic)	rs121909064
ClinGen	rs121909064
ebi	rs121909064
HLI	rs121909064
Exac	rs121909064
Gnomad	rs121909064
Varsome	rs121909064
LitVar	rs121909064
Map	rs121909064
PheGenI	rs121909064
Biobank	rs121909064
1000 genomes	rs121909064
hgdp	rs121909064
ensembl	rs121909064
geneview	rs121909064
scholar	rs121909064
google	rs121909064
pharmgkb	rs121909064
gwascentral	rs121909064
openSNP	rs121909064
23andMe	rs121909064
SNPshot	rs121909064
SNPdbe	rs121909064
MSV3d	rs121909064
GWAS Ctlg	rs121909064

Status

Merged into rs121909061

Max Magnitude

0

OMIM	602574
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121909064(C;C)
Alt	rs121909064(C;C)
Reference	Rs121909064(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	TECTA
CLNDBN	Deafness, autosomal dominant 12
Reversed	0
HGVS	NC_000011.9:g.121037412T>C
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000027638.1,