rs2298948

Orientation

minus

Stabilized

minus

Make rs2298948(A;A)

Make rs2298948(A;G)

Make rs2298948(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

75699439

Gene

GCFC2

is a	snp
is	mentioned by
dbSNP	rs2298948
dbSNP (classic)	rs2298948
ClinGen	rs2298948
ebi	rs2298948
HLI	rs2298948
Exac	rs2298948
Gnomad	rs2298948
Varsome	rs2298948
LitVar	rs2298948
Map	rs2298948
PheGenI	rs2298948
Biobank	rs2298948
1000 genomes	rs2298948
hgdp	rs2298948
ensembl	rs2298948
geneview	rs2298948
scholar	rs2298948
google	rs2298948
pharmgkb	rs2298948
gwascentral	rs2298948
openSNP	rs2298948
23andMe	rs2298948
SNPshot	rs2298948
SNPdbe	rs2298948
MSV3d	rs2298948
GWAS Ctlg	rs2298948

GMAF

0.2764

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 22745009]
Trait
Title	Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele	C
P-val	5E-8
Odds Ratio	None None