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

rs397516326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516326(-;-)
Make rs397516326(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position77208777
GeneMYO7A
is asnp
is mentioned by
dbSNPrs397516326
ebirs397516326
HLIrs397516326
Exacrs397516326
Varsomers397516326
Maprs397516326
PheGenIrs397516326
hapmaprs397516326
1000 genomesrs397516326
hgdprs397516326
ensemblrs397516326
gopubmedrs397516326
geneviewrs397516326
scholarrs397516326
googlers397516326
pharmgkbrs397516326
gwascentralrs397516326
openSNPrs397516326
23andMers397516326
23andMe allrs397516326
SNP Nexus

SNPshotrs397516326
SNPdbers397516326
MSV3drs397516326
GWAS Ctlgrs397516326
Max Magnitude0
ClinVar
Risk rs397516326(;)
Alt rs397516326(;)
Reference rs397516326(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76919822delG
CLNSRC ClinVar
CLNACC RCV000036218.4,