Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516316

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516316(A;G)
Make rs397516316(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position77204065
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516316
ebirs397516316
HLIrs397516316
Exacrs397516316
Varsomers397516316
Maprs397516316
PheGenIrs397516316
hapmaprs397516316
1000 genomesrs397516316
hgdprs397516316
ensemblrs397516316
gopubmedrs397516316
geneviewrs397516316
scholarrs397516316
googlers397516316
pharmgkbrs397516316
gwascentralrs397516316
openSNPrs397516316
23andMers397516316
23andMe allrs397516316
SNP Nexus

SNPshotrs397516316
SNPdbers397516316
MSV3drs397516316
GWAS Ctlgrs397516316
Max Magnitude0
ClinVar
Risk rs397516316(G;G)
Alt rs397516316(G;G)
Reference rs397516316(A;A)
Significance Probable-Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76915110A>G
CLNSRC
CLNACC RCV000036185.2,