Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909058(A;G)
Make rs121909058(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position121168076
GeneTECTA
is asnp
is mentioned by
dbSNPrs121909058
ebirs121909058
HLIrs121909058
Exacrs121909058
Varsomers121909058
Maprs121909058
PheGenIrs121909058
hapmaprs121909058
1000 genomesrs121909058
hgdprs121909058
ensemblrs121909058
gopubmedrs121909058
geneviewrs121909058
scholarrs121909058
googlers121909058
pharmgkbrs121909058
gwascentralrs121909058
openSNPrs121909058
23andMers121909058
23andMe allrs121909058
SNP Nexus

SNPshotrs121909058
SNPdbers121909058
MSV3drs121909058
GWAS Ctlgrs121909058
Merged fromRs28939690
Max Magnitude0
OMIM602574
Desc
Variant0002
Relatedalso
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
CLNACC RCV000007429.2,