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rs397515411

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515411(C;C)
Make rs397515411(C;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position78109309
GeneCIB2
is asnp
is mentioned by
dbSNPrs397515411
ebirs397515411
HLIrs397515411
Exacrs397515411
Varsomers397515411
Maprs397515411
PheGenIrs397515411
hapmaprs397515411
1000 genomesrs397515411
hgdprs397515411
ensemblrs397515411
gopubmedrs397515411
geneviewrs397515411
scholarrs397515411
googlers397515411
pharmgkbrs397515411
gwascentralrs397515411
openSNPrs397515411
23andMers397515411
23andMe allrs397515411
SNP Nexus

SNPshotrs397515411
SNPdbers397515411
MSV3drs397515411
GWAS Ctlgrs397515411
Max Magnitude0
ClinVar
Risk rs397515411(C;C)
Alt rs397515411(C;C)
Reference rs397515411(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene CIB2
CLNDBN Deafness, autosomal recessive 48
Reversed 1
HGVS NC_000015.9:g.78401651A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032887.3,