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rs7727656

From SNPedia

Orientationplus
Stabilizedplus
Make rs7727656(G;G)
Make rs7727656(G;T)
Make rs7727656(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position25760570
is asnp
is mentioned by
dbSNPrs7727656
ebirs7727656
HLIrs7727656
Exacrs7727656
Varsomers7727656
Maprs7727656
PheGenIrs7727656
hapmaprs7727656
1000 genomesrs7727656
hgdprs7727656
ensemblrs7727656
gopubmedrs7727656
geneviewrs7727656
scholarrs7727656
googlers7727656
pharmgkbrs7727656
gwascentralrs7727656
openSNPrs7727656
23andMers7727656
23andMe allrs7727656
SNP Nexus

SNPshotrs7727656
SNPdbers7727656
MSV3drs7727656
GWAS Ctlgrs7727656
GMAF0.4206
Max Magnitude
? (G;G) (G;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
rs7727656
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.546875
summary