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rs398123297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123297(-;-)
Make rs398123297(-;T)
Make rs398123297(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position100273304
GenePCCA
is asnp
is mentioned by
dbSNPrs398123297
ebirs398123297
HLIrs398123297
Exacrs398123297
Varsomers398123297
Maprs398123297
PheGenIrs398123297
hapmaprs398123297
1000 genomesrs398123297
hgdprs398123297
ensemblrs398123297
gopubmedrs398123297
geneviewrs398123297
scholarrs398123297
googlers398123297
pharmgkbrs398123297
gwascentralrs398123297
openSNPrs398123297
23andMers398123297
23andMe allrs398123297
SNP Nexus

SNPshotrs398123297
SNPdbers398123297
MSV3drs398123297
GWAS Ctlgrs398123297
Max Magnitude0
ClinVar
Risk rs398123297(T;T)
Alt rs398123297(T;T)
Reference rs398123297(;)
Significance Pathogenic
Disease not provided Propionic acidemia
Variation info
Gene PCCA
CLNDBN not provided Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.100925558dupT
CLNSRC ClinVar
CLNACC RCV000078546.3, RCV000174236.1,