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rs397516301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516301(A;A)
Make rs397516301(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77189412
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516301
ebirs397516301
HLIrs397516301
Exacrs397516301
Varsomers397516301
Maprs397516301
PheGenIrs397516301
hapmaprs397516301
1000 genomesrs397516301
hgdprs397516301
ensemblrs397516301
gopubmedrs397516301
geneviewrs397516301
scholarrs397516301
googlers397516301
pharmgkbrs397516301
gwascentralrs397516301
openSNPrs397516301
23andMers397516301
23andMe allrs397516301
SNP Nexus

SNPshotrs397516301
SNPdbers397516301
MSV3drs397516301
GWAS Ctlgrs397516301
Max Magnitude0
ClinVar
Risk rs397516301(A;A)
Alt rs397516301(A;A)
Reference rs397516301(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76900457G>A
CLNSRC ClinVar
CLNACC RCV000036116.2,