Have questions? Visit https://www.reddit.com/r/SNPedia

rs10874639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs10874639(A;G)
Make rs10874639(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position102668353
is asnp
is mentioned by
dbSNPrs10874639
ebirs10874639
HLIrs10874639
Exacrs10874639
Varsomers10874639
Maprs10874639
PheGenIrs10874639
hapmaprs10874639
1000 genomesrs10874639
hgdprs10874639
ensemblrs10874639
gopubmedrs10874639
geneviewrs10874639
scholarrs10874639
googlers10874639
pharmgkbrs10874639
gwascentralrs10874639
openSNPrs10874639
23andMers10874639
23andMe allrs10874639
SNP Nexus

SNPshotrs10874639
SNPdbers10874639
MSV3drs10874639
GWAS Ctlgrs10874639
GMAF0.1295
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Fibrinogen protein levels


GET Evidence
rs10874639
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.166667
summary