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rs878853112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCAACTCTGCAGAGCAGC;CCAACTCTGCAGAGCAGC) 0 common in clinvar
Make rs878853112(-;-)
Make rs878853112(-;CCAACTCTGCAGAGCAGC)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position98875554
GeneFBXL4
is asnp
is mentioned by
dbSNPrs878853112
dbSNP (old)rs878853112
ClinGenrs878853112
ebirs878853112
HLIrs878853112
Exacrs878853112
Varsomers878853112
Maprs878853112
PheGenIrs878853112
Biobankrs878853112
1000 genomesrs878853112
hgdprs878853112
ensemblrs878853112
gopubmedrs878853112
geneviewrs878853112
scholarrs878853112
googlers878853112
pharmgkbrs878853112
gwascentralrs878853112
openSNPrs878853112
23andMers878853112
23andMe allrs878853112
SNP Nexus

SNPshotrs878853112
SNPdbers878853112
MSV3drs878853112
GWAS Ctlgrs878853112
Max Magnitude0
ClinVar
Risk rs878853112(-;-)
Alt rs878853112(-;-)
Reference Rs878853112(CCAACTCTGCAGAGCAGC;CCAACTCTGCAGAGCAGC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBXL4
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.99323430_99323447delGCTGCTCTGCAGAGTTGG
CLNSRC
CLNACC RCV000224120.1,