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rs878853378

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853378(A;A)
Make rs878853378(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position77174796
GeneMYO7A
is asnp
is mentioned by
dbSNPrs878853378
ebirs878853378
HLIrs878853378
Exacrs878853378
Varsomers878853378
Maprs878853378
PheGenIrs878853378
hapmaprs878853378
1000 genomesrs878853378
hgdprs878853378
ensemblrs878853378
gopubmedrs878853378
geneviewrs878853378
scholarrs878853378
googlers878853378
pharmgkbrs878853378
gwascentralrs878853378
openSNPrs878853378
23andMers878853378
23andMe allrs878853378
SNP Nexus

SNPshotrs878853378
SNPdbers878853378
MSV3drs878853378
GWAS Ctlgrs878853378
Max Magnitude0
ClinVar
Risk rs878853378(A;A)
Alt rs878853378(A;A)
Reference rs878853378(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene MYO7A
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000011.9:g.76885842C>A
CLNSRC
CLNACC RCV000225435.1,