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rs878855334

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878855334(A;T)
Make rs878855334(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position88077224
GeneCEP290
is asnp
is mentioned by
dbSNPrs878855334
ebirs878855334
HLIrs878855334
Exacrs878855334
Varsomers878855334
Maprs878855334
PheGenIrs878855334
hapmaprs878855334
1000 genomesrs878855334
hgdprs878855334
ensemblrs878855334
gopubmedrs878855334
geneviewrs878855334
scholarrs878855334
googlers878855334
pharmgkbrs878855334
gwascentralrs878855334
openSNPrs878855334
23andMers878855334
23andMe allrs878855334
SNP Nexus

SNPshotrs878855334
SNPdbers878855334
MSV3drs878855334
GWAS Ctlgrs878855334
Max Magnitude0
ClinVar
Risk rs878855334(T;T)
Alt rs878855334(T;T)
Reference rs878855334(A;A)
Significance Pathogenic
Disease Nephronophthisis
Variation info
Gene CEP290
CLNDBN Nephronophthisis
Reversed 1
HGVS NC_000012.11:g.88471001T>A
CLNSRC
CLNACC RCV000234827.1,