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rs878853011

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853011(C;T)
Make rs878853011(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position8360361
GeneRERE
is asnp
is mentioned by
dbSNPrs878853011
ebirs878853011
HLIrs878853011
Exacrs878853011
Varsomers878853011
Maprs878853011
PheGenIrs878853011
hapmaprs878853011
1000 genomesrs878853011
hgdprs878853011
ensemblrs878853011
gopubmedrs878853011
geneviewrs878853011
scholarrs878853011
googlers878853011
pharmgkbrs878853011
gwascentralrs878853011
openSNPrs878853011
23andMers878853011
23andMe allrs878853011
SNP Nexus

SNPshotrs878853011
SNPdbers878853011
MSV3drs878853011
GWAS Ctlgrs878853011
Max Magnitude0
ClinVar
Risk rs878853011(T;T)
Alt rs878853011(T;T)
Reference rs878853011(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RERE
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.8420421G>A
CLNSRC
CLNACC RCV000224127.1,