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rs372404688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372404688(A;A)
Make rs372404688(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position49861863
GenePNKP
is asnp
is mentioned by
dbSNPrs372404688
dbSNP (classic)rs372404688
ClinGenrs372404688
ebirs372404688
HLIrs372404688
Exacrs372404688
Gnomadrs372404688
Varsomers372404688
LitVarrs372404688
Maprs372404688
PheGenIrs372404688
Biobankrs372404688
1000 genomesrs372404688
hgdprs372404688
ensemblrs372404688
geneviewrs372404688
scholarrs372404688
googlers372404688
pharmgkbrs372404688
gwascentralrs372404688
openSNPrs372404688
23andMers372404688
SNPshotrs372404688
SNPdbers372404688
MSV3drs372404688
GWAS Ctlgrs372404688
Max Magnitude0
ClinVar
Risk rs372404688(A;A)
Alt rs372404688(A;A)
Reference Rs372404688(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.50365120G>A
CLNSRC
CLNACC RCV000420352.1,