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rs118169528

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118169528(G;T)
Make rs118169528(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100368504
GenePCCA
is asnp
is mentioned by
dbSNPrs118169528
ebirs118169528
HLIrs118169528
Exacrs118169528
Varsomers118169528
Maprs118169528
PheGenIrs118169528
hapmaprs118169528
1000 genomesrs118169528
hgdprs118169528
ensemblrs118169528
gopubmedrs118169528
geneviewrs118169528
scholarrs118169528
googlers118169528
pharmgkbrs118169528
gwascentralrs118169528
openSNPrs118169528
23andMers118169528
23andMe allrs118169528
SNP Nexus

SNPshotrs118169528
SNPdbers118169528
MSV3drs118169528
GWAS Ctlgrs118169528
Max Magnitude0
ClinVar
Risk rs118169528(T;T)
Alt rs118169528(T;T)
Reference rs118169528(G;G)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101020758G>T
CLNSRC
CLNACC RCV000236220.1,