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rs397516320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397516320(-;-)
Make rs397516320(-;C)
Make rs397516320(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position77205562
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516320
ebirs397516320
HLIrs397516320
Exacrs397516320
Varsomers397516320
Maprs397516320
PheGenIrs397516320
hapmaprs397516320
1000 genomesrs397516320
hgdprs397516320
ensemblrs397516320
gopubmedrs397516320
geneviewrs397516320
scholarrs397516320
googlers397516320
pharmgkbrs397516320
gwascentralrs397516320
openSNPrs397516320
23andMers397516320
23andMe allrs397516320
SNP Nexus

SNPshotrs397516320
SNPdbers397516320
MSV3drs397516320
GWAS Ctlgrs397516320
Max Magnitude0
ClinVar
Risk rs397516320(C;C)
Alt rs397516320(C;C)
Reference rs397516320(;)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76916607dupC
CLNSRC ClinVar
CLNACC RCV000036194.2,