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rs397516283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516283(A;A)
Make rs397516283(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77160283
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516283
ebirs397516283
HLIrs397516283
Exacrs397516283
Varsomers397516283
Maprs397516283
PheGenIrs397516283
hapmaprs397516283
1000 genomesrs397516283
hgdprs397516283
ensemblrs397516283
gopubmedrs397516283
geneviewrs397516283
scholarrs397516283
googlers397516283
pharmgkbrs397516283
gwascentralrs397516283
openSNPrs397516283
23andMers397516283
23andMe allrs397516283
SNP Nexus

SNPshotrs397516283
SNPdbers397516283
MSV3drs397516283
GWAS Ctlgrs397516283
Max Magnitude0
ClinVar
Risk rs397516283(A;A)
Alt rs397516283(A;A)
Reference rs397516283(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76871329G>A
CLNSRC ClinVar
CLNACC RCV000036042.2,