Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853225

From SNPedia

Orientationplus
Geno Mag Summary
(GGT;GGT) 0 common in clinvar
Make rs878853225(C;C)
Make rs878853225(C;GGT)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position75858993
GeneMYO6
is asnp
is mentioned by
dbSNPrs878853225
ebirs878853225
HLIrs878853225
Exacrs878853225
Varsomers878853225
Maprs878853225
PheGenIrs878853225
hapmaprs878853225
1000 genomesrs878853225
hgdprs878853225
ensemblrs878853225
gopubmedrs878853225
geneviewrs878853225
scholarrs878853225
googlers878853225
pharmgkbrs878853225
gwascentralrs878853225
openSNPrs878853225
23andMers878853225
23andMe allrs878853225
SNP Nexus

SNPshotrs878853225
SNPdbers878853225
MSV3drs878853225
GWAS Ctlgrs878853225
Max Magnitude0
ClinVar
Risk rs878853225(C;C)
Alt rs878853225(C;C)
Reference rs878853225(GGT;GGT)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO6
CLNDBN Deafness, autosomal dominant 22
Reversed 0
HGVS NC_000006.11:g.76568710_76568712delGGTinsC
CLNSRC
CLNACC RCV000225059.1,