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rs2900976

From SNPedia

Orientationplus
Stabilizedplus
Make rs2900976(C;C)
Make rs2900976(C;T)
Make rs2900976(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position71731350
is asnp
is mentioned by
dbSNPrs2900976
ebirs2900976
HLIrs2900976
Exacrs2900976
Varsomers2900976
Maprs2900976
PheGenIrs2900976
hapmaprs2900976
1000 genomesrs2900976
hgdprs2900976
ensemblrs2900976
gopubmedrs2900976
geneviewrs2900976
scholarrs2900976
googlers2900976
pharmgkbrs2900976
gwascentralrs2900976
openSNPrs2900976
23andMers2900976
23andMe allrs2900976
SNP Nexus

SNPshotrs2900976
SNPdbers2900976
MSV3drs2900976
GWAS Ctlgrs2900976
GMAF0.2296
Max Magnitude
? (C;C) (C;T) (T;T) 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 9.9999999999999995E-7
Odds Ratio NR NR

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


GET Evidence
rs2900976
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.269841
summary