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rs397516317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516317(C;T)
Make rs397516317(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position77204141
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516317
ebirs397516317
HLIrs397516317
Exacrs397516317
Varsomers397516317
Maprs397516317
PheGenIrs397516317
hapmaprs397516317
1000 genomesrs397516317
hgdprs397516317
ensemblrs397516317
gopubmedrs397516317
geneviewrs397516317
scholarrs397516317
googlers397516317
pharmgkbrs397516317
gwascentralrs397516317
openSNPrs397516317
23andMers397516317
23andMe allrs397516317
SNP Nexus

SNPshotrs397516317
SNPdbers397516317
MSV3drs397516317
GWAS Ctlgrs397516317
Max Magnitude0
ClinVar
Risk rs397516317(T;T)
Alt rs397516317(T;T)
Reference rs397516317(C;C)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76915186C>T
CLNSRC ClinVar
CLNACC RCV000036187.2,