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rs397514608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514608(C;T)
Make rs397514608(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position17613696
GeneOTOG
is asnp
is mentioned by
dbSNPrs397514608
ebirs397514608
HLIrs397514608
Exacrs397514608
Varsomers397514608
Maprs397514608
PheGenIrs397514608
hapmaprs397514608
1000 genomesrs397514608
hgdprs397514608
ensemblrs397514608
gopubmedrs397514608
geneviewrs397514608
scholarrs397514608
googlers397514608
pharmgkbrs397514608
gwascentralrs397514608
openSNPrs397514608
23andMers397514608
23andMe allrs397514608
SNP Nexus

SNPshotrs397514608
SNPdbers397514608
MSV3drs397514608
GWAS Ctlgrs397514608
Max Magnitude0
ClinVar
Risk rs397514608(T;T)
Alt rs397514608(T;T)
Reference rs397514608(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOG
CLNDBN Deafness, autosomal recessive 18b
Reversed 0
HGVS NC_000011.9:g.17635243C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033040.3,