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rs796052850

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052850(C;T)
Make rs796052850(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49864205
GenePNKP
is asnp
is mentioned by
dbSNPrs796052850
ebirs796052850
HLIrs796052850
Exacrs796052850
Varsomers796052850
Maprs796052850
PheGenIrs796052850
hapmaprs796052850
1000 genomesrs796052850
hgdprs796052850
ensemblrs796052850
gopubmedrs796052850
geneviewrs796052850
scholarrs796052850
googlers796052850
pharmgkbrs796052850
gwascentralrs796052850
openSNPrs796052850
23andMers796052850
23andMe allrs796052850
SNP Nexus

SNPshotrs796052850
SNPdbers796052850
MSV3drs796052850
GWAS Ctlgrs796052850
Max Magnitude0
ClinVar
Risk rs796052850(T;T)
Alt rs796052850(T;T)
Reference rs796052850(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.50367462G>A
CLNSRC
CLNACC RCV000188430.1,