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rs397516332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516332(A;A)
Make rs397516332(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77214608
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516332
ebirs397516332
HLIrs397516332
Exacrs397516332
Varsomers397516332
Maprs397516332
PheGenIrs397516332
hapmaprs397516332
1000 genomesrs397516332
hgdprs397516332
ensemblrs397516332
gopubmedrs397516332
geneviewrs397516332
scholarrs397516332
googlers397516332
pharmgkbrs397516332
gwascentralrs397516332
openSNPrs397516332
23andMers397516332
23andMe allrs397516332
SNP Nexus

SNPshotrs397516332
SNPdbers397516332
MSV3drs397516332
GWAS Ctlgrs397516332
Max Magnitude0
ClinVar
Risk rs397516332(A,T;A,T)
Alt rs397516332(A,T;A,T)
Reference rs397516332(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76925653G>A
CLNSRC ClinVar
CLNACC RCV000036241.2,