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rs796052026

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052026(A;A)
Make rs796052026(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136327718
GenePCCB
is asnp
is mentioned by
dbSNPrs796052026
ebirs796052026
HLIrs796052026
Exacrs796052026
Varsomers796052026
Maprs796052026
PheGenIrs796052026
hapmaprs796052026
1000 genomesrs796052026
hgdprs796052026
ensemblrs796052026
gopubmedrs796052026
geneviewrs796052026
scholarrs796052026
googlers796052026
pharmgkbrs796052026
gwascentralrs796052026
openSNPrs796052026
23andMers796052026
23andMe allrs796052026
SNP Nexus

SNPshotrs796052026
SNPdbers796052026
MSV3drs796052026
GWAS Ctlgrs796052026
Max Magnitude0
ClinVar
Risk rs796052026(A;A)
Alt rs796052026(A;A)
Reference rs796052026(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136046560G>A
CLNSRC
CLNACC RCV000186098.1,