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rs774949844

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs774949844(C;C)
Make rs774949844(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100527696
GenePCCA
is asnp
is mentioned by
dbSNPrs774949844
ebirs774949844
HLIrs774949844
Exacrs774949844
Varsomers774949844
Maprs774949844
PheGenIrs774949844
hapmaprs774949844
1000 genomesrs774949844
hgdprs774949844
ensemblrs774949844
gopubmedrs774949844
geneviewrs774949844
scholarrs774949844
googlers774949844
pharmgkbrs774949844
gwascentralrs774949844
openSNPrs774949844
23andMers774949844
23andMe allrs774949844
SNP Nexus

SNPshotrs774949844
SNPdbers774949844
MSV3drs774949844
GWAS Ctlgrs774949844
Max Magnitude0
ClinVar
Risk rs774949844(C;C)
Alt rs774949844(C;C)
Reference rs774949844(T;T)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101179950T>C
CLNSRC
CLNACC RCV000236842.1,