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rs878854415

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854415(A;G)
Make rs878854415(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18144495
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878854415
ebirs878854415
HLIrs878854415
Exacrs878854415
Varsomers878854415
Maprs878854415
PheGenIrs878854415
hapmaprs878854415
1000 genomesrs878854415
hgdprs878854415
ensemblrs878854415
gopubmedrs878854415
geneviewrs878854415
scholarrs878854415
googlers878854415
pharmgkbrs878854415
gwascentralrs878854415
openSNPrs878854415
23andMers878854415
23andMe allrs878854415
SNP Nexus

SNPshotrs878854415
SNPdbers878854415
MSV3drs878854415
GWAS Ctlgrs878854415
Max Magnitude0
ClinVar
Risk rs878854415(G;G)
Alt rs878854415(G;G)
Reference rs878854415(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18047809A>G
CLNSRC
CLNACC RCV000227956.1,