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rs796052861

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052861(-;CGCCAGGT)
Make rs796052861(CGCCAGGT;CGCCAGGT)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49861769
GenePNKP
is asnp
is mentioned by
dbSNPrs796052861
dbSNP (old)rs796052861
ClinGenrs796052861
ebirs796052861
HLIrs796052861
Exacrs796052861
Varsomers796052861
Maprs796052861
PheGenIrs796052861
Biobankrs796052861
1000 genomesrs796052861
hgdprs796052861
ensemblrs796052861
gopubmedrs796052861
geneviewrs796052861
scholarrs796052861
googlers796052861
pharmgkbrs796052861
gwascentralrs796052861
openSNPrs796052861
23andMers796052861
23andMe allrs796052861
SNP Nexus

SNPshotrs796052861
SNPdbers796052861
MSV3drs796052861
GWAS Ctlgrs796052861
Max Magnitude0
ClinVar
Risk rs796052861(CGCCAGGT;CGCCAGGT)
Alt rs796052861(CGCCAGGT;CGCCAGGT)
Reference Rs796052861(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.50365027_50365034dupACCTGGCG
CLNSRC
CLNACC RCV000188472.1,