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rs397516324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516324(C;C)
Make rs397516324(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156776
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516324
ebirs397516324
HLIrs397516324
Exacrs397516324
Varsomers397516324
Maprs397516324
PheGenIrs397516324
hapmaprs397516324
1000 genomesrs397516324
hgdprs397516324
ensemblrs397516324
gopubmedrs397516324
geneviewrs397516324
scholarrs397516324
googlers397516324
pharmgkbrs397516324
gwascentralrs397516324
openSNPrs397516324
23andMers397516324
23andMe allrs397516324
SNP Nexus

SNPshotrs397516324
SNPdbers397516324
MSV3drs397516324
GWAS Ctlgrs397516324
Max Magnitude0
ClinVar
Risk rs397516324(C;C)
Alt rs397516324(C;C)
Reference rs397516324(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867822T>C
CLNSRC ClinVar
CLNACC RCV000036211.2,