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rs1373549

From SNPedia

Orientationminus
Stabilizedminus
Make rs1373549(C;C)
Make rs1373549(C;T)
Make rs1373549(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position46092055
is asnp
is mentioned by
dbSNPrs1373549
ebirs1373549
HLIrs1373549
Exacrs1373549
Varsomers1373549
Maprs1373549
PheGenIrs1373549
hapmaprs1373549
1000 genomesrs1373549
hgdprs1373549
ensemblrs1373549
gopubmedrs1373549
geneviewrs1373549
scholarrs1373549
googlers1373549
pharmgkbrs1373549
gwascentralrs1373549
openSNPrs1373549
23andMers1373549
23andMe allrs1373549
SNP Nexus

SNPshotrs1373549
SNPdbers1373549
MSV3drs1373549
GWAS Ctlgrs1373549
GMAF0.3058
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000008
Odds Ratio NR NR


GET Evidence
rs1373549
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.664062
summary