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rs11254363

From SNPedia

Orientationplus
Stabilizedplus
Make rs11254363(A;A)
Make rs11254363(A;G)
Make rs11254363(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position17088694
GeneCUBN
is asnp
is mentioned by
dbSNPrs11254363
ebirs11254363
HLIrs11254363
Exacrs11254363
Varsomers11254363
Maprs11254363
PheGenIrs11254363
hapmaprs11254363
1000 genomesrs11254363
hgdprs11254363
ensemblrs11254363
gopubmedrs11254363
geneviewrs11254363
scholarrs11254363
googlers11254363
pharmgkbrs11254363
gwascentralrs11254363
openSNPrs11254363
23andMers11254363
23andMe allrs11254363
SNP Nexus

SNPshotrs11254363
SNPdbers11254363
MSV3drs11254363
GWAS Ctlgrs11254363
GMAF0.2144
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19303062OA-icon.png]
Trait Folate pathway vitamins
Title Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations
Risk Allele A
P-val 0.000001
Odds Ratio 21.49 [7.71-35.27] pg/mL decrease



GET Evidence
rs11254363
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.257812
summary