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rs1888414

From SNPedia

Orientationplus
Stabilizedplus
Make rs1888414(C;C)
Make rs1888414(C;T)
Make rs1888414(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position20405418
is asnp
is mentioned by
dbSNPrs1888414
ebirs1888414
HLIrs1888414
Exacrs1888414
Varsomers1888414
Maprs1888414
PheGenIrs1888414
hapmaprs1888414
1000 genomesrs1888414
hgdprs1888414
ensemblrs1888414
gopubmedrs1888414
geneviewrs1888414
scholarrs1888414
googlers1888414
pharmgkbrs1888414
gwascentralrs1888414
openSNPrs1888414
23andMers1888414
23andMe allrs1888414
SNP Nexus

SNPshotrs1888414
SNPdbers1888414
MSV3drs1888414
GWAS Ctlgrs1888414
GMAF0.3641
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 2E-7
Odds Ratio NR NR


GET Evidence
rs1888414
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.601562
summary