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rs377385081

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377385081(A;A)
Make rs377385081(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position18145938
GeneMYO15A
is asnp
is mentioned by
dbSNPrs377385081
ebirs377385081
HLIrs377385081
Exacrs377385081
Varsomers377385081
Maprs377385081
PheGenIrs377385081
hapmaprs377385081
1000 genomesrs377385081
hgdprs377385081
ensemblrs377385081
gopubmedrs377385081
geneviewrs377385081
scholarrs377385081
googlers377385081
pharmgkbrs377385081
gwascentralrs377385081
openSNPrs377385081
23andMers377385081
23andMe allrs377385081
SNP Nexus

SNPshotrs377385081
SNPdbers377385081
MSV3drs377385081
GWAS Ctlgrs377385081
Max Magnitude0
ClinVar
Risk rs377385081(A;A)
Alt rs377385081(A;A)
Reference rs377385081(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18049252G>A
CLNSRC
CLNACC RCV000225063.1,