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rs2298948

From SNPedia

Orientationminus
Stabilizedminus
Make rs2298948(A;A)
Make rs2298948(A;G)
Make rs2298948(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position75699439
GeneGCFC2
is asnp
is mentioned by
dbSNPrs2298948
ebirs2298948
HLIrs2298948
Exacrs2298948
Varsomers2298948
Maprs2298948
PheGenIrs2298948
hapmaprs2298948
1000 genomesrs2298948
hgdprs2298948
ensemblrs2298948
gopubmedrs2298948
geneviewrs2298948
scholarrs2298948
googlers2298948
pharmgkbrs2298948
gwascentralrs2298948
openSNPrs2298948
23andMers2298948
23andMe allrs2298948
SNP Nexus

SNPshotrs2298948
SNPdbers2298948
MSV3drs2298948
GWAS Ctlgrs2298948
GMAF0.2764
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele C
P-val 5E-8
Odds Ratio None None