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rs397516294

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516294(-;-)
Make rs397516294(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77175449
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516294
ebirs397516294
HLIrs397516294
Exacrs397516294
Varsomers397516294
Maprs397516294
PheGenIrs397516294
hapmaprs397516294
1000 genomesrs397516294
hgdprs397516294
ensemblrs397516294
gopubmedrs397516294
geneviewrs397516294
scholarrs397516294
googlers397516294
pharmgkbrs397516294
gwascentralrs397516294
openSNPrs397516294
23andMers397516294
23andMe allrs397516294
SNP Nexus

SNPshotrs397516294
SNPdbers397516294
MSV3drs397516294
GWAS Ctlgrs397516294
Max Magnitude0
ClinVar
Risk rs397516294(;)
Alt rs397516294(;)
Reference rs397516294(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76886495delC
CLNSRC ClinVar
CLNACC RCV000036078.2,