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rs397516310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516310(C;C)
Make rs397516310(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77197568
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516310
ebirs397516310
HLIrs397516310
Exacrs397516310
Varsomers397516310
Maprs397516310
PheGenIrs397516310
hapmaprs397516310
1000 genomesrs397516310
hgdprs397516310
ensemblrs397516310
gopubmedrs397516310
geneviewrs397516310
scholarrs397516310
googlers397516310
pharmgkbrs397516310
gwascentralrs397516310
openSNPrs397516310
23andMers397516310
23andMe allrs397516310
SNP Nexus

SNPshotrs397516310
SNPdbers397516310
MSV3drs397516310
GWAS Ctlgrs397516310
Max Magnitude0
ClinVar
Risk rs397516310(C;C)
Alt rs397516310(C;C)
Reference rs397516310(T;T)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76908613T>C
CLNSRC ClinVar
CLNACC RCV000036143.2,