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rs878854411

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854411(C;T)
Make rs878854411(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18131308
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878854411
ebirs878854411
HLIrs878854411
Exacrs878854411
Varsomers878854411
Maprs878854411
PheGenIrs878854411
hapmaprs878854411
1000 genomesrs878854411
hgdprs878854411
ensemblrs878854411
gopubmedrs878854411
geneviewrs878854411
scholarrs878854411
googlers878854411
pharmgkbrs878854411
gwascentralrs878854411
openSNPrs878854411
23andMers878854411
23andMe allrs878854411
SNP Nexus

SNPshotrs878854411
SNPdbers878854411
MSV3drs878854411
GWAS Ctlgrs878854411
Max Magnitude0
ClinVar
Risk rs878854411(T;T)
Alt rs878854411(T;T)
Reference rs878854411(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18034622C>T
CLNSRC
CLNACC RCV000229545.1,