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rs878853227

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853227(G;T)
Make rs878853227(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18149575
GeneLOC105371568, MYO15A
is asnp
is mentioned by
dbSNPrs878853227
ebirs878853227
HLIrs878853227
Exacrs878853227
Varsomers878853227
Maprs878853227
PheGenIrs878853227
hapmaprs878853227
1000 genomesrs878853227
hgdprs878853227
ensemblrs878853227
gopubmedrs878853227
geneviewrs878853227
scholarrs878853227
googlers878853227
pharmgkbrs878853227
gwascentralrs878853227
openSNPrs878853227
23andMers878853227
23andMe allrs878853227
SNP Nexus

SNPshotrs878853227
SNPdbers878853227
MSV3drs878853227
GWAS Ctlgrs878853227
Max Magnitude0
ClinVar
Risk rs878853227(T;T)
Alt rs878853227(T;T)
Reference rs878853227(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18052889G>T
CLNSRC
CLNACC RCV000225053.1,