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rs878853270

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853270(C;G)
Make rs878853270(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position8358750
GeneRERE
is asnp
is mentioned by
dbSNPrs878853270
ebirs878853270
HLIrs878853270
Exacrs878853270
Varsomers878853270
Maprs878853270
PheGenIrs878853270
hapmaprs878853270
1000 genomesrs878853270
hgdprs878853270
ensemblrs878853270
gopubmedrs878853270
geneviewrs878853270
scholarrs878853270
googlers878853270
pharmgkbrs878853270
gwascentralrs878853270
openSNPrs878853270
23andMers878853270
23andMe allrs878853270
SNP Nexus

SNPshotrs878853270
SNPdbers878853270
MSV3drs878853270
GWAS Ctlgrs878853270
Max Magnitude0
ClinVar
Risk rs878853270(G;G)
Alt rs878853270(G;G)
Reference rs878853270(C;C)
Significance Pathogenic
Disease Neurodevelopmental disorder with or without anomalies of the brain
Variation info
Gene RERE
CLNDBN Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart
Reversed 1
HGVS NC_000001.10:g.8418810G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000225240.1,