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rs121909060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909060(C;C)
Make rs121909060(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position121160301
GeneTECTA
is asnp
is mentioned by
dbSNPrs121909060
ebirs121909060
HLIrs121909060
Exacrs121909060
Varsomers121909060
Maprs121909060
PheGenIrs121909060
hapmaprs121909060
1000 genomesrs121909060
hgdprs121909060
ensemblrs121909060
gopubmedrs121909060
geneviewrs121909060
scholarrs121909060
googlers121909060
pharmgkbrs121909060
gwascentralrs121909060
openSNPrs121909060
23andMers121909060
23andMe allrs121909060
SNP Nexus

SNPshotrs121909060
SNPdbers121909060
MSV3drs121909060
GWAS Ctlgrs121909060
Merged fromRs28939691
Max Magnitude0
OMIM602574
Desc
Variant0005
Relatedalso
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
CLNACC RCV000007432.2,