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rs397516322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516322(A;A)
Make rs397516322(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77205599
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516322
ebirs397516322
HLIrs397516322
Exacrs397516322
Varsomers397516322
Maprs397516322
PheGenIrs397516322
hapmaprs397516322
1000 genomesrs397516322
hgdprs397516322
ensemblrs397516322
gopubmedrs397516322
geneviewrs397516322
scholarrs397516322
googlers397516322
pharmgkbrs397516322
gwascentralrs397516322
openSNPrs397516322
23andMers397516322
23andMe allrs397516322
SNP Nexus

SNPshotrs397516322
SNPdbers397516322
MSV3drs397516322
GWAS Ctlgrs397516322
Max Magnitude0
ClinVar
Risk rs397516322(A;A)
Alt rs397516322(A;A)
Reference rs397516322(G;G)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76916644G>A
CLNSRC ClinVar
CLNACC RCV000036197.2,