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rs782384464

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782384464(A;A)
Make rs782384464(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77179073
GeneMYO7A
is asnp
is mentioned by
dbSNPrs782384464
ebirs782384464
HLIrs782384464
Exacrs782384464
Varsomers782384464
Maprs782384464
PheGenIrs782384464
hapmaprs782384464
1000 genomesrs782384464
hgdprs782384464
ensemblrs782384464
gopubmedrs782384464
geneviewrs782384464
scholarrs782384464
googlers782384464
pharmgkbrs782384464
gwascentralrs782384464
openSNPrs782384464
23andMers782384464
23andMe allrs782384464
SNP Nexus

SNPshotrs782384464
SNPdbers782384464
MSV3drs782384464
GWAS Ctlgrs782384464
Max Magnitude0
ClinVar
Risk rs782384464(A;A)
Alt rs782384464(A;A)
Reference rs782384464(G;G)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene MYO7A
CLNDBN Usher syndrome, type 1
Reversed 0
HGVS NC_000011.9:g.76890119G>T
CLNSRC
CLNACC RCV000216077.1,