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rs767645983

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767645983(G;G)
Make rs767645983(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position49861883
GenePNKP
is asnp
is mentioned by
dbSNPrs767645983
ebirs767645983
HLIrs767645983
Exacrs767645983
Varsomers767645983
Maprs767645983
PheGenIrs767645983
hapmaprs767645983
1000 genomesrs767645983
hgdprs767645983
ensemblrs767645983
gopubmedrs767645983
geneviewrs767645983
scholarrs767645983
googlers767645983
pharmgkbrs767645983
gwascentralrs767645983
openSNPrs767645983
23andMers767645983
23andMe allrs767645983
SNP Nexus

SNPshotrs767645983
SNPdbers767645983
MSV3drs767645983
GWAS Ctlgrs767645983
Max Magnitude0
ClinVar
Risk rs767645983(G;G)
Alt rs767645983(G;G)
Reference rs767645983(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PNKP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.50365140T>G
CLNSRC
CLNACC RCV000188450.1,