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rs2295639

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs2295639(A;G)
Make rs2295639(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position64435398
GeneMTHFD1
is asnp
is mentioned by
dbSNPrs2295639
ebirs2295639
HLIrs2295639
Exacrs2295639
Varsomers2295639
Maprs2295639
PheGenIrs2295639
hapmaprs2295639
1000 genomesrs2295639
hgdprs2295639
ensemblrs2295639
gopubmedrs2295639
geneviewrs2295639
scholarrs2295639
googlers2295639
pharmgkbrs2295639
gwascentralrs2295639
openSNPrs2295639
23andMers2295639
23andMe allrs2295639
SNP Nexus

SNPshotrs2295639
SNPdbers2295639
MSV3drs2295639
GWAS Ctlgrs2295639
GMAF0.05005
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19734545OA-icon.png]
Trait Cognitive performance
Title A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery
Risk Allele
P-val 0.000005
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 5 x 10^-6) for spatial working memory (SWM) strategy in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs2295639
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0703125
summary