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rs878854414

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854414(A;A)
Make rs878854414(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18143969
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878854414
ebirs878854414
HLIrs878854414
Exacrs878854414
Varsomers878854414
Maprs878854414
PheGenIrs878854414
hapmaprs878854414
1000 genomesrs878854414
hgdprs878854414
ensemblrs878854414
gopubmedrs878854414
geneviewrs878854414
scholarrs878854414
googlers878854414
pharmgkbrs878854414
gwascentralrs878854414
openSNPrs878854414
23andMers878854414
23andMe allrs878854414
SNP Nexus

SNPshotrs878854414
SNPdbers878854414
MSV3drs878854414
GWAS Ctlgrs878854414
Max Magnitude0
ClinVar
Risk rs878854414(A;A)
Alt rs878854414(A;A)
Reference rs878854414(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18047283C>A
CLNSRC
CLNACC RCV000233062.1,