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rs397516331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516331(A;A)
Make rs397516331(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77213919
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516331
ebirs397516331
HLIrs397516331
Exacrs397516331
Varsomers397516331
Maprs397516331
PheGenIrs397516331
hapmaprs397516331
1000 genomesrs397516331
hgdprs397516331
ensemblrs397516331
gopubmedrs397516331
geneviewrs397516331
scholarrs397516331
googlers397516331
pharmgkbrs397516331
gwascentralrs397516331
openSNPrs397516331
23andMers397516331
23andMe allrs397516331
SNP Nexus

SNPshotrs397516331
SNPdbers397516331
MSV3drs397516331
GWAS Ctlgrs397516331
Max Magnitude0
ClinVar
Risk rs397516331(A;A)
Alt rs397516331(A;A)
Reference rs397516331(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76924964C>A
CLNSRC ClinVar
CLNACC RCV000036236.2,