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rs121965083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965083(A;A)
Make rs121965083(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77172834
GeneMYO7A
is asnp
is mentioned by
dbSNPrs121965083
ebirs121965083
HLIrs121965083
Exacrs121965083
Varsomers121965083
Maprs121965083
PheGenIrs121965083
hapmaprs121965083
1000 genomesrs121965083
hgdprs121965083
ensemblrs121965083
gopubmedrs121965083
geneviewrs121965083
scholarrs121965083
googlers121965083
pharmgkbrs121965083
gwascentralrs121965083
openSNPrs121965083
23andMers121965083
23andMe allrs121965083
SNP Nexus

SNPshotrs121965083
SNPdbers121965083
MSV3drs121965083
GWAS Ctlgrs121965083
Max Magnitude0
OMIM276903
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121965083(A;A)
Alt rs121965083(A;A)
Reference rs121965083(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1B
Reversed 0
HGVS NC_000011.9:g.76883880C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012633.17,