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rs796052025

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052025(G;T)
Make rs796052025(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position136255931
GenePCCB
is asnp
is mentioned by
dbSNPrs796052025
ebirs796052025
HLIrs796052025
Exacrs796052025
Varsomers796052025
Maprs796052025
PheGenIrs796052025
hapmaprs796052025
1000 genomesrs796052025
hgdprs796052025
ensemblrs796052025
gopubmedrs796052025
geneviewrs796052025
scholarrs796052025
googlers796052025
pharmgkbrs796052025
gwascentralrs796052025
openSNPrs796052025
23andMers796052025
23andMe allrs796052025
SNP Nexus

SNPshotrs796052025
SNPdbers796052025
MSV3drs796052025
GWAS Ctlgrs796052025
Max Magnitude0
ClinVar
Risk rs796052025(T;T)
Alt rs796052025(T;T)
Reference rs796052025(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.135974773G>T
CLNSRC
CLNACC RCV000186097.1,