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rs886044667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position21728372
GeneOTOA
is asnp
is mentioned by
dbSNPrs886044667
dbSNP (classic)rs886044667
ClinGenrs886044667
ebirs886044667
HLIrs886044667
Exacrs886044667
Gnomadrs886044667
Varsomers886044667
LitVarrs886044667
Maprs886044667
PheGenIrs886044667
Biobankrs886044667
1000 genomesrs886044667
hgdprs886044667
ensemblrs886044667
geneviewrs886044667
scholarrs886044667
googlers886044667
pharmgkbrs886044667
gwascentralrs886044667
openSNPrs886044667
23andMers886044667
SNPshotrs886044667
SNPdbers886044667
MSV3drs886044667
GWAS Ctlgrs886044667
Max Magnitude0
ClinVar
Risk rs886044667(A;A)
Alt rs886044667(A;A)
Reference Rs886044667(C;C)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene OTOA
CLNDBN Deafness, autosomal recessive 22
Reversed 0
HGVS NC_000016.9:g.21739693C>A
CLNSRC
CLNACC RCV000303562.1,