Have questions? Visit https://www.reddit.com/r/SNPedia

rs772727116

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772727116(C;T)
Make rs772727116(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49862408
GenePNKP
is asnp
is mentioned by
dbSNPrs772727116
ebirs772727116
HLIrs772727116
Exacrs772727116
Varsomers772727116
Maprs772727116
PheGenIrs772727116
hapmaprs772727116
1000 genomesrs772727116
hgdprs772727116
ensemblrs772727116
gopubmedrs772727116
geneviewrs772727116
scholarrs772727116
googlers772727116
pharmgkbrs772727116
gwascentralrs772727116
openSNPrs772727116
23andMers772727116
23andMe allrs772727116
SNP Nexus

SNPshotrs772727116
SNPdbers772727116
MSV3drs772727116
GWAS Ctlgrs772727116
Max Magnitude0
ClinVar
Risk rs772727116(T;T)
Alt rs772727116(T;T)
Reference rs772727116(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.50365665C>T
CLNSRC
CLNACC RCV000188442.2,