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rs397516312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516312(A;A)
Make rs397516312(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77156079
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516312
ebirs397516312
HLIrs397516312
Exacrs397516312
Varsomers397516312
Maprs397516312
PheGenIrs397516312
hapmaprs397516312
1000 genomesrs397516312
hgdprs397516312
ensemblrs397516312
gopubmedrs397516312
geneviewrs397516312
scholarrs397516312
googlers397516312
pharmgkbrs397516312
gwascentralrs397516312
openSNPrs397516312
23andMers397516312
23andMe allrs397516312
SNP Nexus

SNPshotrs397516312
SNPdbers397516312
MSV3drs397516312
GWAS Ctlgrs397516312
Max Magnitude0
ClinVar
Risk rs397516312(A,T;A,T)
Alt rs397516312(A,T;A,T)
Reference rs397516312(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76867125G>A
CLNSRC ClinVar
CLNACC RCV000036154.2,