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rs878854402

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878854402(A;G)
Make rs878854402(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position177033050
GeneTBL1XR1
is asnp
is mentioned by
dbSNPrs878854402
ebirs878854402
HLIrs878854402
Exacrs878854402
Varsomers878854402
Maprs878854402
PheGenIrs878854402
hapmaprs878854402
1000 genomesrs878854402
hgdprs878854402
ensemblrs878854402
gopubmedrs878854402
geneviewrs878854402
scholarrs878854402
googlers878854402
pharmgkbrs878854402
gwascentralrs878854402
openSNPrs878854402
23andMers878854402
23andMe allrs878854402
SNP Nexus

SNPshotrs878854402
SNPdbers878854402
MSV3drs878854402
GWAS Ctlgrs878854402
Max Magnitude0
ClinVar
Risk rs878854402(G;G)
Alt rs878854402(G;G)
Reference rs878854402(A;A)
Significance Pathogenic
Disease Pierpont syndrome
Variation info
Gene TBL1XR1
CLNDBN Pierpont syndrome
Reversed 1
HGVS NC_000003.11:g.176750838T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000211104.1,