Have questions? Visit https://www.reddit.com/r/SNPedia

rs4727380

From SNPedia

Orientationplus
Stabilizedplus
Make rs4727380(C;C)
Make rs4727380(C;G)
Make rs4727380(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position77416489
GeneGSAP, RP5-899E9.1
is asnp
is mentioned by
dbSNPrs4727380
ebirs4727380
HLIrs4727380
Exacrs4727380
Varsomers4727380
Maprs4727380
PheGenIrs4727380
hapmaprs4727380
1000 genomesrs4727380
hgdprs4727380
ensemblrs4727380
gopubmedrs4727380
geneviewrs4727380
scholarrs4727380
googlers4727380
pharmgkbrs4727380
gwascentralrs4727380
openSNPrs4727380
23andMers4727380
23andMe allrs4727380
SNP Nexus

SNPshotrs4727380
SNPdbers4727380
MSV3drs4727380
GWAS Ctlgrs4727380
Max Magnitude

[PMID 25037285] A common GSAP promoter variant contributes to Alzheimer's disease liability