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rs397507445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGGCATCATCCGGC;GGGCATCATCCGGC) 0 common in clinvar
Make rs397507445(GGGCATCATCCGGC;TAGAGCACAGGA)
Make rs397507445(TAGAGCACAGGA;TAGAGCACAGGA)
ReferenceGRCh38 38.1/141
Chromosome3
Position136327174
GenePCCB
is asnp
is mentioned by
dbSNPrs397507445
dbSNP (old)rs397507445
ClinGenrs397507445
ebirs397507445
HLIrs397507445
Exacrs397507445
Gnomadrs397507445
Varsomers397507445
Maprs397507445
PheGenIrs397507445
Biobankrs397507445
1000 genomesrs397507445
hgdprs397507445
ensemblrs397507445
gopubmedrs397507445
geneviewrs397507445
scholarrs397507445
googlers397507445
pharmgkbrs397507445
gwascentralrs397507445
openSNPrs397507445
23andMers397507445
23andMe allrs397507445
SNP Nexus

SNPshotrs397507445
SNPdbers397507445
MSV3drs397507445
GWAS Ctlgrs397507445
Max Magnitude0
ClinVar
Risk rs397507445(TAGAGCACAGGA;TAGAGCACAGGA)
Alt rs397507445(TAGAGCACAGGA;TAGAGCACAGGA)
Reference Rs397507445(GGGCATCATCCGGC;GGGCATCATCCGGC)
Significance Pathogenic
Disease Propionic acidemia not provided
Variation info
Gene PCCB
CLNDBN Propionic acidemia not provided
Reversed 0
HGVS NC_000003.11:g.136046016_136046029delGGGCATCATCCGGCinsTAGAGCACAGGA
CLNSRC GTR
CLNACC RCV000032124.2, RCV000370248.1,