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rs121908965

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908965(A;T)
Make rs121908965(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18145935
GeneMYO15A
is asnp
is mentioned by
dbSNPrs121908965
ebirs121908965
HLIrs121908965
Exacrs121908965
Varsomers121908965
Maprs121908965
PheGenIrs121908965
hapmaprs121908965
1000 genomesrs121908965
hgdprs121908965
ensemblrs121908965
gopubmedrs121908965
geneviewrs121908965
scholarrs121908965
googlers121908965
pharmgkbrs121908965
gwascentralrs121908965
openSNPrs121908965
23andMers121908965
23andMe allrs121908965
SNP Nexus

SNPshotrs121908965
SNPdbers121908965
MSV3drs121908965
GWAS Ctlgrs121908965
Max Magnitude0
OMIM602666
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908965(T;T)
Alt rs121908965(T;T)
Reference rs121908965(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO15A
CLNDBN Deafness, autosomal recessive 3
Reversed 0
HGVS NC_000017.10:g.18049249A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007365.2,