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rs369982920

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369982920(A;A)
Make rs369982920(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100515567
GenePCCA
is asnp
is mentioned by
dbSNPrs369982920
ebirs369982920
HLIrs369982920
Exacrs369982920
Varsomers369982920
Maprs369982920
PheGenIrs369982920
hapmaprs369982920
1000 genomesrs369982920
hgdprs369982920
ensemblrs369982920
gopubmedrs369982920
geneviewrs369982920
scholarrs369982920
googlers369982920
pharmgkbrs369982920
gwascentralrs369982920
openSNPrs369982920
23andMers369982920
23andMe allrs369982920
SNP Nexus

SNPshotrs369982920
SNPdbers369982920
MSV3drs369982920
GWAS Ctlgrs369982920
Max Magnitude0
ClinVar
Risk rs369982920(A;A)
Alt rs369982920(A;A)
Reference rs369982920(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101167821G>A
CLNSRC
CLNACC RCV000236921.1,