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rs878853238

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853238(A;A)
Make rs878853238(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18156202
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878853238
ebirs878853238
HLIrs878853238
Exacrs878853238
Varsomers878853238
Maprs878853238
PheGenIrs878853238
hapmaprs878853238
1000 genomesrs878853238
hgdprs878853238
ensemblrs878853238
gopubmedrs878853238
geneviewrs878853238
scholarrs878853238
googlers878853238
pharmgkbrs878853238
gwascentralrs878853238
openSNPrs878853238
23andMers878853238
23andMe allrs878853238
SNP Nexus

SNPshotrs878853238
SNPdbers878853238
MSV3drs878853238
GWAS Ctlgrs878853238
Max Magnitude0
ClinVar
Risk rs878853238(A;A)
Alt rs878853238(A;A)
Reference rs878853238(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18059516G>A
CLNSRC
CLNACC RCV000225089.1,