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rs797044729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044729(-;AAGATCTGCAAA)
Make rs797044729(AAGATCTGCAAA;AAGATCTGCAAA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136260535
GenePCCB
is asnp
is mentioned by
dbSNPrs797044729
ClinGenrs797044729
ebirs797044729
HLIrs797044729
Exacrs797044729
Varsomers797044729
Maprs797044729
PheGenIrs797044729
hapmaprs797044729
1000 genomesrs797044729
hgdprs797044729
ensemblrs797044729
gopubmedrs797044729
geneviewrs797044729
scholarrs797044729
googlers797044729
pharmgkbrs797044729
gwascentralrs797044729
openSNPrs797044729
23andMers797044729
23andMe allrs797044729
SNP Nexus

SNPshotrs797044729
SNPdbers797044729
MSV3drs797044729
GWAS Ctlgrs797044729
Max Magnitude0
ClinVar
Risk rs797044729(AAAAGATCTGCA;AAAAGATCTGCA)
Alt rs797044729(AAAAGATCTGCA;AAAAGATCTGCA)
Reference Rs797044729(-;-)
Significance Pathogenic
Disease Propionic acidemia
Variation info
Gene PCCB
CLNDBN Propionic acidemia
Reversed 0
HGVS NC_000003.11:g.135979366_135979377dupAAGATCTGCAAA
CLNSRC
CLNACC RCV000178114.1,