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rs794727334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTAA;GTAA) 0 common in clinvar
Make rs794727334(-;-)
Make rs794727334(-;AGTA)
Make rs794727334(AGTA;AGTA)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100449309
GenePCCA
is asnp
is mentioned by
dbSNPrs794727334
ClinGenrs794727334
ebirs794727334
HLIrs794727334
Exacrs794727334
Varsomers794727334
Maprs794727334
PheGenIrs794727334
hapmaprs794727334
1000 genomesrs794727334
hgdprs794727334
ensemblrs794727334
gopubmedrs794727334
geneviewrs794727334
scholarrs794727334
googlers794727334
pharmgkbrs794727334
gwascentralrs794727334
openSNPrs794727334
23andMers794727334
23andMe allrs794727334
SNP Nexus

SNPshotrs794727334
SNPdbers794727334
MSV3drs794727334
GWAS Ctlgrs794727334
Max Magnitude0
ClinVar
Risk rs794727334(-;-)
Alt rs794727334(-;-)
Reference Rs794727334(GTAA;GTAA)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCA
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000013.10:g.101101563_101101566delAGTA
CLNSRC
CLNACC RCV000176154.1,