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rs8192708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs8192708(A;G)
Make rs8192708(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position57563565
GenePCK1
is asnp
is mentioned by
dbSNPrs8192708
ebirs8192708
HLIrs8192708
Exacrs8192708
Varsomers8192708
Maprs8192708
PheGenIrs8192708
hapmaprs8192708
1000 genomesrs8192708
hgdprs8192708
ensemblrs8192708
gopubmedrs8192708
geneviewrs8192708
scholarrs8192708
googlers8192708
pharmgkbrs8192708
gwascentralrs8192708
openSNPrs8192708
23andMers8192708
23andMe allrs8192708
SNP Nexus

SNPshotrs8192708
SNPdbers8192708
MSV3drs8192708
GWAS Ctlgrs8192708
GMAF0.06795
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21152065OA-icon.png] A Putative Alzheimer's Disease Risk Allele in PCK1 Influences Brain Atrophy in Multiple Sclerosis


[PMID 18780302OA-icon.png] Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.


[PMID 18813964OA-icon.png] Alzheimer's disease risk variants show association with cerebrospinal fluid amyloid beta.


[PMID 18830724OA-icon.png] Assessment of Alzheimer's disease case-control associations using family-based methods.


[PMID 20574532OA-icon.png] Intermediate phenotypes identify divergent pathways to Alzheimer's disease.


GET Evidence
PCK1-I267V
aa_change Ile267Val
aa_change_short I267V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0980666
summary