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rs3814219

From SNPedia

Orientationplus
Stabilizedplus
Make rs3814219(A;A)
Make rs3814219(A;G)
Make rs3814219(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position103887337
GeneOBFC1
is asnp
is mentioned by
dbSNPrs3814219
ebirs3814219
HLIrs3814219
Exacrs3814219
Varsomers3814219
Maprs3814219
PheGenIrs3814219
hapmaprs3814219
1000 genomesrs3814219
hgdprs3814219
ensemblrs3814219
gopubmedrs3814219
geneviewrs3814219
scholarrs3814219
googlers3814219
pharmgkbrs3814219
gwascentralrs3814219
openSNPrs3814219
23andMers3814219
23andMe allrs3814219
SNP Nexus

SNPshotrs3814219
SNPdbers3814219
MSV3drs3814219
GWAS Ctlgrs3814219
GMAF0.2094
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 17903301OA-icon.png] BA baseline flow, rs3814219 (OBFC1, 9.48*10(-7))
GWAS
SNP rs3814219
PubMedID [PMID 17903301OA-icon.png]
Condition Endothelial function traits
Gene OBFC1
Risk Allele
pValue 9.00E-007
OR NA
95% CI



[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


[PMID 20421499OA-icon.png] Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.


GET Evidence
rs3814219
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary