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rs2877832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs2877832(C;T)
Make rs2877832(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position27330971
GeneMFSD1
is asnp
is mentioned by
dbSNPrs2877832
ebirs2877832
HLIrs2877832
Exacrs2877832
Varsomers2877832
Maprs2877832
PheGenIrs2877832
hapmaprs2877832
1000 genomesrs2877832
hgdprs2877832
ensemblrs2877832
gopubmedrs2877832
geneviewrs2877832
scholarrs2877832
googlers2877832
pharmgkbrs2877832
gwascentralrs2877832
openSNPrs2877832
23andMers2877832
23andMe allrs2877832
SNP Nexus

SNPshotrs2877832
SNPdbers2877832
MSV3drs2877832
GWAS Ctlgrs2877832
GMAF0.06612
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs2877832
PubMedID [PMID 17903298OA-icon.png]
Condition Diabetes related insulin traits
Gene Intergenic
Risk Allele
pValue 3.00E-006
OR NA
95% CI




GET Evidence
rs2877832
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary