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rs12044355

From SNPedia

Orientationplus
Stabilizedplus
Make rs12044355(A;A)
Make rs12044355(A;C)
Make rs12044355(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position231708601
GeneDISC1, MAP1LC3C
is asnp
is mentioned by
dbSNPrs12044355
ebirs12044355
HLIrs12044355
Exacrs12044355
Varsomers12044355
Maprs12044355
PheGenIrs12044355
hapmaprs12044355
1000 genomesrs12044355
hgdprs12044355
ensemblrs12044355
gopubmedrs12044355
geneviewrs12044355
scholarrs12044355
googlers12044355
pharmgkbrs12044355
gwascentralrs12044355
openSNPrs12044355
23andMers12044355
23andMe allrs12044355
SNP Nexus

SNPshotrs12044355
SNPdbers12044355
MSV3drs12044355
GWAS Ctlgrs12044355
GMAF0.3255
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19118814OA-icon.png]
Trait Alzheimer's disease
Title Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease
Risk Allele
P-val 0.000009
Odds Ratio NR NR




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


GET Evidence
rs12044355
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary