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rs10498514

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10498514(A;C)
Make rs10498514(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position64432337
GeneMTHFD1
is asnp
is mentioned by
dbSNPrs10498514
ebirs10498514
HLIrs10498514
Exacrs10498514
Varsomers10498514
Maprs10498514
PheGenIrs10498514
hapmaprs10498514
1000 genomesrs10498514
hgdprs10498514
ensemblrs10498514
gopubmedrs10498514
geneviewrs10498514
scholarrs10498514
googlers10498514
pharmgkbrs10498514
gwascentralrs10498514
openSNPrs10498514
23andMers10498514
23andMe allrs10498514
SNP Nexus

SNPshotrs10498514
SNPdbers10498514
MSV3drs10498514
GWAS Ctlgrs10498514
GMAF0.05831
Max Magnitude0
? (A;A) (A;C) (C;C) 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 8E-7
Odds Ratio NR NR

[PMID 19734545OA-icon.png] non sig. gwas, hit (p = 8 x 10^-7) for spatial working memory (SWM) strategy in the CANTAB (Cambridge Neuropsychological Test Automated Battery)


GET Evidence
rs10498514
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary