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rs172881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs172881(C;T)
Make rs172881(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position41107378
is asnp
is mentioned by
dbSNPrs172881
ebirs172881
HLIrs172881
Exacrs172881
Varsomers172881
Maprs172881
PheGenIrs172881
hapmaprs172881
1000 genomesrs172881
hgdprs172881
ensemblrs172881
gopubmedrs172881
geneviewrs172881
scholarrs172881
googlers172881
pharmgkbrs172881
gwascentralrs172881
openSNPrs172881
23andMers172881
23andMe allrs172881
SNP Nexus

SNPshotrs172881
SNPdbers172881
MSV3drs172881
GWAS Ctlgrs172881
Merged fromRs1103125
Max Magnitude0

[PMID 20522590OA-icon.png] Functional variants in MBL2 are associated with type 2 diabetes and pre-diabetes traits in Pima Indians and the old order Amish.