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rs796052022

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052022(-;-)
Make rs796052022(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136297950
GenePCCB
is asnp
is mentioned by
dbSNPrs796052022
ebirs796052022
HLIrs796052022
Exacrs796052022
Varsomers796052022
Maprs796052022
PheGenIrs796052022
hapmaprs796052022
1000 genomesrs796052022
hgdprs796052022
ensemblrs796052022
gopubmedrs796052022
geneviewrs796052022
scholarrs796052022
googlers796052022
pharmgkbrs796052022
gwascentralrs796052022
openSNPrs796052022
23andMers796052022
23andMe allrs796052022
SNP Nexus

SNPshotrs796052022
SNPdbers796052022
MSV3drs796052022
GWAS Ctlgrs796052022
Max Magnitude0
ClinVar
Risk rs796052022(;)
Alt rs796052022(;)
Reference rs796052022(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136016792delA
CLNSRC
CLNACC RCV000186092.1,