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rs878854413

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854413(-;-)
Make rs878854413(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18140640
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878854413
ebirs878854413
HLIrs878854413
Exacrs878854413
Varsomers878854413
Maprs878854413
PheGenIrs878854413
hapmaprs878854413
1000 genomesrs878854413
hgdprs878854413
ensemblrs878854413
gopubmedrs878854413
geneviewrs878854413
scholarrs878854413
googlers878854413
pharmgkbrs878854413
gwascentralrs878854413
openSNPrs878854413
23andMers878854413
23andMe allrs878854413
SNP Nexus

SNPshotrs878854413
SNPdbers878854413
MSV3drs878854413
GWAS Ctlgrs878854413
Max Magnitude0
ClinVar
Risk rs878854413(;)
Alt rs878854413(;)
Reference rs878854413(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18043954delC
CLNSRC
CLNACC RCV000227379.1,