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rs771438170

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771438170(A;A)
Make rs771438170(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100515529
GenePCCA
is asnp
is mentioned by
dbSNPrs771438170
ebirs771438170
HLIrs771438170
Exacrs771438170
Varsomers771438170
Maprs771438170
PheGenIrs771438170
hapmaprs771438170
1000 genomesrs771438170
hgdprs771438170
ensemblrs771438170
gopubmedrs771438170
geneviewrs771438170
scholarrs771438170
googlers771438170
pharmgkbrs771438170
gwascentralrs771438170
openSNPrs771438170
23andMers771438170
23andMe allrs771438170
SNP Nexus

SNPshotrs771438170
SNPdbers771438170
MSV3drs771438170
GWAS Ctlgrs771438170
Max Magnitude0
ClinVar
Risk rs771438170(A;A)
Alt rs771438170(A;A)
Reference rs771438170(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101167783G>A
CLNSRC
CLNACC RCV000235940.1,