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rs397516291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516291(C;T)
Make rs397516291(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77174783
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516291
ebirs397516291
HLIrs397516291
Exacrs397516291
Varsomers397516291
Maprs397516291
PheGenIrs397516291
hapmaprs397516291
1000 genomesrs397516291
hgdprs397516291
ensemblrs397516291
gopubmedrs397516291
geneviewrs397516291
scholarrs397516291
googlers397516291
pharmgkbrs397516291
gwascentralrs397516291
openSNPrs397516291
23andMers397516291
23andMe allrs397516291
SNP Nexus

SNPshotrs397516291
SNPdbers397516291
MSV3drs397516291
GWAS Ctlgrs397516291
Max Magnitude0
ClinVar
Risk rs397516291(T;T)
Alt rs397516291(T;T)
Reference rs397516291(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76885829C>T
CLNSRC ClinVar
CLNACC RCV000036071.2,