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rs727503467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503467(A;A)
Make rs727503467(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position121187987
GeneTECTA
is asnp
is mentioned by
dbSNPrs727503467
dbSNP (classic)rs727503467
ClinGenrs727503467
ebirs727503467
HLIrs727503467
Exacrs727503467
Gnomadrs727503467
Varsomers727503467
LitVarrs727503467
Maprs727503467
PheGenIrs727503467
Biobankrs727503467
1000 genomesrs727503467
hgdprs727503467
ensemblrs727503467
geneviewrs727503467
scholarrs727503467
googlers727503467
pharmgkbrs727503467
gwascentralrs727503467
openSNPrs727503467
23andMers727503467
SNPshotrs727503467
SNPdbers727503467
MSV3drs727503467
GWAS Ctlgrs727503467
Max Magnitude0
ClinVar
Risk rs727503467(A;A)
Alt rs727503467(A;A)
Reference Rs727503467(G;G)
Significance Probable-Pathogenic
Disease Nonsyndromic hearing loss and deafness
Variation info
Gene TECTA
CLNDBN Nonsyndromic hearing loss and deafness
Reversed 0
HGVS NC_000011.9:g.121058696G>A
CLNSRC
CLNACC RCV000151989.1,