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rs202247814

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202247814(A;A)
Make rs202247814(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position100155090
GenePCCA
is asnp
is mentioned by
dbSNPrs202247814
ebirs202247814
HLIrs202247814
Exacrs202247814
Varsomers202247814
Maprs202247814
PheGenIrs202247814
hapmaprs202247814
1000 genomesrs202247814
hgdprs202247814
ensemblrs202247814
gopubmedrs202247814
geneviewrs202247814
scholarrs202247814
googlers202247814
pharmgkbrs202247814
gwascentralrs202247814
openSNPrs202247814
23andMers202247814
23andMe allrs202247814
SNP Nexus

SNPshotrs202247814
SNPdbers202247814
MSV3drs202247814
GWAS Ctlgrs202247814
Max Magnitude0
ClinVar
Risk rs202247814(A;A)
Alt rs202247814(A;A)
Reference rs202247814(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.100807344G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032110.1,