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rs796052021

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796052021(-;-)
Make rs796052021(-;G)
Make rs796052021(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136283942
GenePCCB
is asnp
is mentioned by
dbSNPrs796052021
ebirs796052021
HLIrs796052021
Exacrs796052021
Varsomers796052021
Maprs796052021
PheGenIrs796052021
hapmaprs796052021
1000 genomesrs796052021
hgdprs796052021
ensemblrs796052021
gopubmedrs796052021
geneviewrs796052021
scholarrs796052021
googlers796052021
pharmgkbrs796052021
gwascentralrs796052021
openSNPrs796052021
23andMers796052021
23andMe allrs796052021
SNP Nexus

SNPshotrs796052021
SNPdbers796052021
MSV3drs796052021
GWAS Ctlgrs796052021
Max Magnitude0
ClinVar
Risk rs796052021(G;G)
Alt rs796052021(G;G)
Reference rs796052021(;)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136002784dupG
CLNSRC
CLNACC RCV000186091.1,