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rs397516285

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516285(A;A)
Make rs397516285(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77147806
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516285
ebirs397516285
HLIrs397516285
Exacrs397516285
Varsomers397516285
Maprs397516285
PheGenIrs397516285
hapmaprs397516285
1000 genomesrs397516285
hgdprs397516285
ensemblrs397516285
gopubmedrs397516285
geneviewrs397516285
scholarrs397516285
googlers397516285
pharmgkbrs397516285
gwascentralrs397516285
openSNPrs397516285
23andMers397516285
23andMe allrs397516285
SNP Nexus

SNPshotrs397516285
SNPdbers397516285
MSV3drs397516285
GWAS Ctlgrs397516285
Max Magnitude0
ClinVar
Risk rs397516285(A;A)
Alt rs397516285(A;A)
Reference rs397516285(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76858852G>A
CLNSRC ClinVar
CLNACC RCV000036050.2,