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rs878853226

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853226(C;T)
Make rs878853226(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position30885994
GeneCOCH, LOC100506071
is asnp
is mentioned by
dbSNPrs878853226
ebirs878853226
HLIrs878853226
Exacrs878853226
Varsomers878853226
Maprs878853226
PheGenIrs878853226
hapmaprs878853226
1000 genomesrs878853226
hgdprs878853226
ensemblrs878853226
gopubmedrs878853226
geneviewrs878853226
scholarrs878853226
googlers878853226
pharmgkbrs878853226
gwascentralrs878853226
openSNPrs878853226
23andMers878853226
23andMe allrs878853226
SNP Nexus

SNPshotrs878853226
SNPdbers878853226
MSV3drs878853226
GWAS Ctlgrs878853226
Max Magnitude0
ClinVar
Risk rs878853226(T;T)
Alt rs878853226(T;T)
Reference rs878853226(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene COCH LOC100506071
CLNDBN Deafness, autosomal dominant 9
Reversed 0
HGVS NC_000014.8:g.31355200C>T
CLNSRC
CLNACC RCV000225026.1,