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rs796052859

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052859(-;T)
Make rs796052859(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49864211
GenePNKP
is asnp
is mentioned by
dbSNPrs796052859
dbSNP (old)rs796052859
ClinGenrs796052859
ebirs796052859
HLIrs796052859
Exacrs796052859
Varsomers796052859
Maprs796052859
PheGenIrs796052859
Biobankrs796052859
1000 genomesrs796052859
hgdprs796052859
ensemblrs796052859
gopubmedrs796052859
geneviewrs796052859
scholarrs796052859
googlers796052859
pharmgkbrs796052859
gwascentralrs796052859
openSNPrs796052859
23andMers796052859
23andMe allrs796052859
SNP Nexus

SNPshotrs796052859
SNPdbers796052859
MSV3drs796052859
GWAS Ctlgrs796052859
Max Magnitude0
ClinVar
Risk rs796052859(T;T)
Alt rs796052859(T;T)
Reference Rs796052859(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.50367469dupA
CLNSRC
CLNACC RCV000188468.2,