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rs878853408

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853408(C;G)
Make rs878853408(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position216246733
GeneUSH2A
is asnp
is mentioned by
dbSNPrs878853408
ebirs878853408
HLIrs878853408
Exacrs878853408
Varsomers878853408
Maprs878853408
PheGenIrs878853408
hapmaprs878853408
1000 genomesrs878853408
hgdprs878853408
ensemblrs878853408
gopubmedrs878853408
geneviewrs878853408
scholarrs878853408
googlers878853408
pharmgkbrs878853408
gwascentralrs878853408
openSNPrs878853408
23andMers878853408
23andMe allrs878853408
SNP Nexus

SNPshotrs878853408
SNPdbers878853408
MSV3drs878853408
GWAS Ctlgrs878853408
Max Magnitude0
ClinVar
Risk rs878853408(G;G)
Alt rs878853408(G;G)
Reference rs878853408(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene USH2A
CLNDBN Retinal dystrophy
Reversed 1
HGVS NC_000001.10:g.216420075G>C
CLNSRC
CLNACC RCV000225384.1,