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rs199919568

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199919568(A;G)
Make rs199919568(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49862369
GenePNKP
is asnp
is mentioned by
dbSNPrs199919568
ebirs199919568
HLIrs199919568
Exacrs199919568
Varsomers199919568
Maprs199919568
PheGenIrs199919568
hapmaprs199919568
1000 genomesrs199919568
hgdprs199919568
ensemblrs199919568
gopubmedrs199919568
geneviewrs199919568
scholarrs199919568
googlers199919568
pharmgkbrs199919568
gwascentralrs199919568
openSNPrs199919568
23andMers199919568
23andMe allrs199919568
SNP Nexus

SNPshotrs199919568
SNPdbers199919568
MSV3drs199919568
GWAS Ctlgrs199919568
Max Magnitude0
ClinVar
Risk rs199919568(G;G)
Alt rs199919568(G;G)
Reference rs199919568(A;A)
Significance Pathogenic
Disease not specified
Variation info
Gene PNKP
CLNDBN not specified
Reversed 0
HGVS NC_000019.9:g.50365626A>G
CLNSRC
CLNACC RCV000188445.2,