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rs878854410

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854410(A;A)
Make rs878854410(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18127077
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878854410
ebirs878854410
HLIrs878854410
Exacrs878854410
Varsomers878854410
Maprs878854410
PheGenIrs878854410
hapmaprs878854410
1000 genomesrs878854410
hgdprs878854410
ensemblrs878854410
gopubmedrs878854410
geneviewrs878854410
scholarrs878854410
googlers878854410
pharmgkbrs878854410
gwascentralrs878854410
openSNPrs878854410
23andMers878854410
23andMe allrs878854410
SNP Nexus

SNPshotrs878854410
SNPdbers878854410
MSV3drs878854410
GWAS Ctlgrs878854410
Max Magnitude0
ClinVar
Risk rs878854410(A;A)
Alt rs878854410(A;A)
Reference rs878854410(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18030391G>A
CLNSRC
CLNACC RCV000226627.1,