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rs7561273

From SNPedia

Orientationplus
Stabilizedplus
Make rs7561273(A;A)
Make rs7561273(A;G)
Make rs7561273(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position24024644
GeneMFSD2B
is asnp
is mentioned by
dbSNPrs7561273
ebirs7561273
HLIrs7561273
Exacrs7561273
Varsomers7561273
Maprs7561273
PheGenIrs7561273
hapmaprs7561273
1000 genomesrs7561273
hgdprs7561273
ensemblrs7561273
gopubmedrs7561273
geneviewrs7561273
scholarrs7561273
googlers7561273
pharmgkbrs7561273
gwascentralrs7561273
openSNPrs7561273
23andMers7561273
23andMe allrs7561273
SNP Nexus

SNPshotrs7561273
SNPdbers7561273
MSV3drs7561273
GWAS Ctlgrs7561273
GMAF0.3884
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele A
P-val 0.000006
Odds Ratio 0.22 [NR] mg/L decrease

C-reactive protein (CRP) levels being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs7561273
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.601562
summary