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rs121965081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965081(C;C)
Make rs121965081(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77157000
GeneMYO7A
is asnp
is mentioned by
dbSNPrs121965081
ebirs121965081
HLIrs121965081
Exacrs121965081
Varsomers121965081
Maprs121965081
PheGenIrs121965081
hapmaprs121965081
1000 genomesrs121965081
hgdprs121965081
ensemblrs121965081
gopubmedrs121965081
geneviewrs121965081
scholarrs121965081
googlers121965081
pharmgkbrs121965081
gwascentralrs121965081
openSNPrs121965081
23andMers121965081
23andMe allrs121965081
SNP Nexus

SNPshotrs121965081
SNPdbers121965081
MSV3drs121965081
GWAS Ctlgrs121965081
Max Magnitude0
OMIM276903
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121965081(A,C;A,C)
Alt rs121965081(A,C;A,C)
Reference rs121965081(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene MYO7A
CLNDBN Deafness, autosomal recessive 2
Reversed 0
HGVS NC_000011.9:g.76868046G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012627.23,