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rs878854409

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854409(C;G)
Make rs878854409(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18119542
GeneLOC105371566, MYO15A
is asnp
is mentioned by
dbSNPrs878854409
ebirs878854409
HLIrs878854409
Exacrs878854409
Varsomers878854409
Maprs878854409
PheGenIrs878854409
hapmaprs878854409
1000 genomesrs878854409
hgdprs878854409
ensemblrs878854409
gopubmedrs878854409
geneviewrs878854409
scholarrs878854409
googlers878854409
pharmgkbrs878854409
gwascentralrs878854409
openSNPrs878854409
23andMers878854409
23andMe allrs878854409
SNP Nexus

SNPshotrs878854409
SNPdbers878854409
MSV3drs878854409
GWAS Ctlgrs878854409
Max Magnitude0
ClinVar
Risk rs878854409(G;G)
Alt rs878854409(G;G)
Reference rs878854409(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18022856C>G
CLNSRC
CLNACC RCV000231728.1,