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rs796052024

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052024(C;C)
Make rs796052024(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136283856
GenePCCB
is asnp
is mentioned by
dbSNPrs796052024
ebirs796052024
HLIrs796052024
Exacrs796052024
Varsomers796052024
Maprs796052024
PheGenIrs796052024
hapmaprs796052024
1000 genomesrs796052024
hgdprs796052024
ensemblrs796052024
gopubmedrs796052024
geneviewrs796052024
scholarrs796052024
googlers796052024
pharmgkbrs796052024
gwascentralrs796052024
openSNPrs796052024
23andMers796052024
23andMe allrs796052024
SNP Nexus

SNPshotrs796052024
SNPdbers796052024
MSV3drs796052024
GWAS Ctlgrs796052024
Max Magnitude0
ClinVar
Risk rs796052024(C;C)
Alt rs796052024(C;C)
Reference rs796052024(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136002698G>C
CLNSRC
CLNACC RCV000186094.1,