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rs147379583

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147379583(A;A)
Make rs147379583(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position136301035
GenePCCB
is asnp
is mentioned by
dbSNPrs147379583
ebirs147379583
HLIrs147379583
Exacrs147379583
Varsomers147379583
Maprs147379583
PheGenIrs147379583
hapmaprs147379583
1000 genomesrs147379583
hgdprs147379583
ensemblrs147379583
gopubmedrs147379583
geneviewrs147379583
scholarrs147379583
googlers147379583
pharmgkbrs147379583
gwascentralrs147379583
openSNPrs147379583
23andMers147379583
23andMe allrs147379583
SNP Nexus

SNPshotrs147379583
SNPdbers147379583
MSV3drs147379583
GWAS Ctlgrs147379583
Max Magnitude0
ClinVar
Risk rs147379583(A,C,T;A,C,T)
Alt rs147379583(A,C,T;A,C,T)
Reference rs147379583(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136019877G>A
CLNSRC
CLNACC RCV000186096.1,