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rs375781731

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375781731(A;A)
Make rs375781731(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49865135
GenePNKP
is asnp
is mentioned by
dbSNPrs375781731
ebirs375781731
HLIrs375781731
Exacrs375781731
Varsomers375781731
Maprs375781731
PheGenIrs375781731
hapmaprs375781731
1000 genomesrs375781731
hgdprs375781731
ensemblrs375781731
gopubmedrs375781731
geneviewrs375781731
scholarrs375781731
googlers375781731
pharmgkbrs375781731
gwascentralrs375781731
openSNPrs375781731
23andMers375781731
23andMe allrs375781731
SNP Nexus

SNPshotrs375781731
SNPdbers375781731
MSV3drs375781731
GWAS Ctlgrs375781731
Max Magnitude0
ClinVar
Risk rs375781731(A;A)
Alt rs375781731(A;A)
Reference rs375781731(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.50368392G>A
CLNSRC
CLNACC RCV000188429.2,