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rs397516315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516315(A;A)
Make rs397516315(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77199787
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516315
ebirs397516315
HLIrs397516315
Exacrs397516315
Varsomers397516315
Maprs397516315
PheGenIrs397516315
hapmaprs397516315
1000 genomesrs397516315
hgdprs397516315
ensemblrs397516315
gopubmedrs397516315
geneviewrs397516315
scholarrs397516315
googlers397516315
pharmgkbrs397516315
gwascentralrs397516315
openSNPrs397516315
23andMers397516315
23andMe allrs397516315
SNP Nexus

SNPshotrs397516315
SNPdbers397516315
MSV3drs397516315
GWAS Ctlgrs397516315
Max Magnitude0
ClinVar
Risk rs397516315(A;A)
Alt rs397516315(A;A)
Reference rs397516315(T;T)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76910832T>A
CLNSRC ClinVar
CLNACC RCV000036166.2,