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rs397516323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516323(C;C)
Make rs397516323(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77207350
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516323
ebirs397516323
HLIrs397516323
Exacrs397516323
Varsomers397516323
Maprs397516323
PheGenIrs397516323
hapmaprs397516323
1000 genomesrs397516323
hgdprs397516323
ensemblrs397516323
gopubmedrs397516323
geneviewrs397516323
scholarrs397516323
googlers397516323
pharmgkbrs397516323
gwascentralrs397516323
openSNPrs397516323
23andMers397516323
23andMe allrs397516323
SNP Nexus

SNPshotrs397516323
SNPdbers397516323
MSV3drs397516323
GWAS Ctlgrs397516323
Max Magnitude0
ClinVar
Risk rs397516323(C;C)
Alt rs397516323(C;C)
Reference rs397516323(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76918395T>C
CLNSRC ClinVar
CLNACC RCV000036203.2,