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rs397516330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516330(A;G)
Make rs397516330(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77213858
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516330
ebirs397516330
HLIrs397516330
Exacrs397516330
Varsomers397516330
Maprs397516330
PheGenIrs397516330
hapmaprs397516330
1000 genomesrs397516330
hgdprs397516330
ensemblrs397516330
gopubmedrs397516330
geneviewrs397516330
scholarrs397516330
googlers397516330
pharmgkbrs397516330
gwascentralrs397516330
openSNPrs397516330
23andMers397516330
23andMe allrs397516330
SNP Nexus

SNPshotrs397516330
SNPdbers397516330
MSV3drs397516330
GWAS Ctlgrs397516330
Max Magnitude0
ClinVar
Risk rs397516330(G;G)
Alt rs397516330(G;G)
Reference rs397516330(A;A)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76924903A>G
CLNSRC ClinVar
CLNACC RCV000036235.2,