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rs368657015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs368657015(C;C)
Make rs368657015(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77205554
GeneMYO7A
is asnp
is mentioned by
dbSNPrs368657015
ebirs368657015
HLIrs368657015
Exacrs368657015
Varsomers368657015
Maprs368657015
PheGenIrs368657015
hapmaprs368657015
1000 genomesrs368657015
hgdprs368657015
ensemblrs368657015
gopubmedrs368657015
geneviewrs368657015
scholarrs368657015
googlers368657015
pharmgkbrs368657015
gwascentralrs368657015
openSNPrs368657015
23andMers368657015
23andMe allrs368657015
SNP Nexus

SNPshotrs368657015
SNPdbers368657015
MSV3drs368657015
GWAS Ctlgrs368657015
Max Magnitude0
ClinVar
Risk rs368657015(C;C)
Alt rs368657015(C;C)
Reference rs368657015(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76916599T>C
CLNSRC ClinVar
CLNACC RCV000036193.3,