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rs61886492

From SNPedia

Orientationplus
Stabilizedplus
Make rs61886492(A;A)
Make rs61886492(A;G)
Make rs61886492(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position49164722
GeneFOLH1
is asnp
is mentioned by
dbSNPrs61886492
ebirs61886492
HLIrs61886492
Exacrs61886492
Varsomers61886492
Maprs61886492
PheGenIrs61886492
hapmaprs61886492
1000 genomesrs61886492
hgdprs61886492
ensemblrs61886492
gopubmedrs61886492
geneviewrs61886492
scholarrs61886492
googlers61886492
pharmgkbrs61886492
gwascentralrs61886492
openSNPrs61886492
23andMers61886492
23andMe allrs61886492
SNP Nexus

SNPshotrs61886492
SNPdbers61886492
MSV3drs61886492
GWAS Ctlgrs61886492
GMAF0.02938
Max Magnitude

[PMID 21597034OA-icon.png] The Folate Hydrolase 1561C>T Polymorphism Is Associated With Depressive Symptoms in Puerto Rican Adults


[PMID 22124883] Glutamate carboxypeptidase II gene polymorphisms and neural tube defects in a high-risk Chinese population

GET Evidence
FOLH1-H475Y
aa_change His475Tyr
aa_change_short H475Y
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.041217
summary



[PMID 24291031] Association of APOE, GCPII and MMP9 polymorphisms with common diseases and lipid levels in an older adult/elderly cohort


[PMID 22918695OA-icon.png] The maternal folate hydrolase gene polymorphism is associated with neural tube defects in a high-risk Chinese population.