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rs10074258

From SNPedia

Orientationplus
Stabilizedplus
Make rs10074258(C;C)
Make rs10074258(C;T)
Make rs10074258(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position107646859
GeneEFNA5
is asnp
is mentioned by
dbSNPrs10074258
ebirs10074258
HLIrs10074258
Exacrs10074258
Varsomers10074258
Maprs10074258
PheGenIrs10074258
hapmaprs10074258
1000 genomesrs10074258
hgdprs10074258
ensemblrs10074258
gopubmedrs10074258
geneviewrs10074258
scholarrs10074258
googlers10074258
pharmgkbrs10074258
gwascentralrs10074258
openSNPrs10074258
23andMers10074258
23andMe allrs10074258
SNP Nexus

SNPshotrs10074258
SNPdbers10074258
MSV3drs10074258
GWAS Ctlgrs10074258
GMAF0.3728
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
rs10074258
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.388889
summary