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rs1364705

From SNPedia

Orientationminus
Stabilizedminus
Make rs1364705(C;C)
Make rs1364705(C;T)
Make rs1364705(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position119212566
GeneMAL2
is asnp
is mentioned by
dbSNPrs1364705
ebirs1364705
HLIrs1364705
Exacrs1364705
Varsomers1364705
Maprs1364705
PheGenIrs1364705
hapmaprs1364705
1000 genomesrs1364705
hgdprs1364705
ensemblrs1364705
gopubmedrs1364705
geneviewrs1364705
scholarrs1364705
googlers1364705
pharmgkbrs1364705
gwascentralrs1364705
openSNPrs1364705
23andMers1364705
23andMe allrs1364705
SNP Nexus

SNPshotrs1364705
SNPdbers1364705
MSV3drs1364705
GWAS Ctlgrs1364705
GMAF0.2755
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 0.000009
Odds Ratio NR NR


GET Evidence
rs1364705
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary