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rs398123463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs398123463(AAC;AAC)
Make rs398123463(AAC;TT)
ReferenceGRCh38 38.1/141
Chromosome3
Position136260492
GenePCCB
is asnp
is mentioned by
dbSNPrs398123463
ebirs398123463
HLIrs398123463
Exacrs398123463
Varsomers398123463
Maprs398123463
PheGenIrs398123463
hapmaprs398123463
1000 genomesrs398123463
hgdprs398123463
ensemblrs398123463
gopubmedrs398123463
geneviewrs398123463
scholarrs398123463
googlers398123463
pharmgkbrs398123463
gwascentralrs398123463
openSNPrs398123463
23andMers398123463
23andMe allrs398123463
SNP Nexus

SNPshotrs398123463
SNPdbers398123463
MSV3drs398123463
GWAS Ctlgrs398123463
Max Magnitude0
ClinVar
Risk rs398123463(AAC;AAC)
Alt rs398123463(AAC;AAC)
Reference rs398123463(TT;TT)
Significance Pathogenic
Disease not provided Propionic acidemia
Variation info
Gene PCCB
CLNDBN not provided Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135979334_135979335delTTinsAAC
CLNSRC ClinVar
CLNACC RCV000079094.3, RCV000178113.1,