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rs878853228

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853228(A;A)
Make rs878853228(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18155225
GeneMYO15A
is asnp
is mentioned by
dbSNPrs878853228
ebirs878853228
HLIrs878853228
Exacrs878853228
Varsomers878853228
Maprs878853228
PheGenIrs878853228
hapmaprs878853228
1000 genomesrs878853228
hgdprs878853228
ensemblrs878853228
gopubmedrs878853228
geneviewrs878853228
scholarrs878853228
googlers878853228
pharmgkbrs878853228
gwascentralrs878853228
openSNPrs878853228
23andMers878853228
23andMe allrs878853228
SNP Nexus

SNPshotrs878853228
SNPdbers878853228
MSV3drs878853228
GWAS Ctlgrs878853228
Max Magnitude0
ClinVar
Risk rs878853228(A;A)
Alt rs878853228(A;A)
Reference rs878853228(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18058539G>A
CLNSRC
CLNACC RCV000225093.1,