Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052020

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052020(A;G)
Make rs796052020(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136293754
GenePCCB
is asnp
is mentioned by
dbSNPrs796052020
ebirs796052020
HLIrs796052020
Exacrs796052020
Varsomers796052020
Maprs796052020
PheGenIrs796052020
hapmaprs796052020
1000 genomesrs796052020
hgdprs796052020
ensemblrs796052020
gopubmedrs796052020
geneviewrs796052020
scholarrs796052020
googlers796052020
pharmgkbrs796052020
gwascentralrs796052020
openSNPrs796052020
23andMers796052020
23andMe allrs796052020
SNP Nexus

SNPshotrs796052020
SNPdbers796052020
MSV3drs796052020
GWAS Ctlgrs796052020
Max Magnitude0
ClinVar
Risk rs796052020(G;G)
Alt rs796052020(G;G)
Reference rs796052020(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136012596A>G
CLNSRC
CLNACC RCV000186086.1,