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rs794727620

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727620(A;A)
Make rs794727620(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100111992
GenePCCA
is asnp
is mentioned by
dbSNPrs794727620
ebirs794727620
HLIrs794727620
Exacrs794727620
Varsomers794727620
Maprs794727620
PheGenIrs794727620
hapmaprs794727620
1000 genomesrs794727620
hgdprs794727620
ensemblrs794727620
gopubmedrs794727620
geneviewrs794727620
scholarrs794727620
googlers794727620
pharmgkbrs794727620
gwascentralrs794727620
openSNPrs794727620
23andMers794727620
23andMe allrs794727620
SNP Nexus

SNPshotrs794727620
SNPdbers794727620
MSV3drs794727620
GWAS Ctlgrs794727620
Max Magnitude0
ClinVar
Risk rs794727620(A;A)
Alt rs794727620(A;A)
Reference rs794727620(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.100764246G>A
CLNSRC
CLNACC RCV000178067.1,