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rs121908966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908966(A;T)
Make rs121908966(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18145929
GeneMYO15A
is asnp
is mentioned by
dbSNPrs121908966
ebirs121908966
HLIrs121908966
Exacrs121908966
Varsomers121908966
Maprs121908966
PheGenIrs121908966
hapmaprs121908966
1000 genomesrs121908966
hgdprs121908966
ensemblrs121908966
gopubmedrs121908966
geneviewrs121908966
scholarrs121908966
googlers121908966
pharmgkbrs121908966
gwascentralrs121908966
openSNPrs121908966
23andMers121908966
23andMe allrs121908966
SNP Nexus

SNPshotrs121908966
SNPdbers121908966
MSV3drs121908966
GWAS Ctlgrs121908966
Max Magnitude0
OMIM602666
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908966(T;T)
Alt rs121908966(T;T)
Reference rs121908966(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18049243A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007366.2,