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rs121965084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121965084(A;T)
Make rs121965084(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77162149
GeneMYO7A
is asnp
is mentioned by
dbSNPrs121965084
ebirs121965084
HLIrs121965084
Exacrs121965084
Varsomers121965084
Maprs121965084
PheGenIrs121965084
hapmaprs121965084
1000 genomesrs121965084
hgdprs121965084
ensemblrs121965084
gopubmedrs121965084
geneviewrs121965084
scholarrs121965084
googlers121965084
pharmgkbrs121965084
gwascentralrs121965084
openSNPrs121965084
23andMers121965084
23andMe allrs121965084
SNP Nexus

SNPshotrs121965084
SNPdbers121965084
MSV3drs121965084
GWAS Ctlgrs121965084
Merged fromRs28934903
Max Magnitude0
OMIM276903
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121965084(G,T;G,T)
Alt rs121965084(G,T;G,T)
Reference rs121965084(A;A)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal dominant 11
Reversed 0
HGVS NC_000011.9:g.76873195A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012638.17,