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rs776496862

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776496862(A;A)
Make rs776496862(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100425674
GenePCCA
is asnp
is mentioned by
dbSNPrs776496862
ebirs776496862
HLIrs776496862
Exacrs776496862
Varsomers776496862
Maprs776496862
PheGenIrs776496862
hapmaprs776496862
1000 genomesrs776496862
hgdprs776496862
ensemblrs776496862
gopubmedrs776496862
geneviewrs776496862
scholarrs776496862
googlers776496862
pharmgkbrs776496862
gwascentralrs776496862
openSNPrs776496862
23andMers776496862
23andMe allrs776496862
SNP Nexus

SNPshotrs776496862
SNPdbers776496862
MSV3drs776496862
GWAS Ctlgrs776496862
Max Magnitude0
ClinVar
Risk rs776496862(A;A)
Alt rs776496862(A;A)
Reference rs776496862(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101077928G>A
CLNSRC
CLNACC RCV000176030.1,