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rs796052023

From SNPedia

Orientationplus
Geno Mag Summary
(TGA;TGA) 0 common in clinvar
Make rs796052023(-;-)
Make rs796052023(-;TGA)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136316949
GenePCCB
is asnp
is mentioned by
dbSNPrs796052023
ebirs796052023
HLIrs796052023
Exacrs796052023
Varsomers796052023
Maprs796052023
PheGenIrs796052023
hapmaprs796052023
1000 genomesrs796052023
hgdprs796052023
ensemblrs796052023
gopubmedrs796052023
geneviewrs796052023
scholarrs796052023
googlers796052023
pharmgkbrs796052023
gwascentralrs796052023
openSNPrs796052023
23andMers796052023
23andMe allrs796052023
SNP Nexus

SNPshotrs796052023
SNPdbers796052023
MSV3drs796052023
GWAS Ctlgrs796052023
Max Magnitude0
ClinVar
Risk rs796052023(;)
Alt rs796052023(;)
Reference rs796052023(TGA;TGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136035791_136035793delTGA
CLNSRC
CLNACC RCV000186093.1,