Have questions? Visit https://www.reddit.com/r/SNPedia

rs121965085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121965085(C;T)
Make rs121965085(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77174816
GeneMYO7A
is asnp
is mentioned by
dbSNPrs121965085
ebirs121965085
HLIrs121965085
Exacrs121965085
Varsomers121965085
Maprs121965085
PheGenIrs121965085
hapmaprs121965085
1000 genomesrs121965085
hgdprs121965085
ensemblrs121965085
gopubmedrs121965085
geneviewrs121965085
scholarrs121965085
googlers121965085
pharmgkbrs121965085
gwascentralrs121965085
openSNPrs121965085
23andMers121965085
23andMe allrs121965085
SNP Nexus

SNPshotrs121965085
SNPdbers121965085
MSV3drs121965085
GWAS Ctlgrs121965085
Max Magnitude0
OMIM276903
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121965085(T;T)
Alt rs121965085(T;T)
Reference rs121965085(C;C)
Significance Pathogenic
Disease Usher syndrome Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1B Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76885862C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012635.23, RCV000151490.1,