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rs1479355

From SNPedia

Orientationplus
Stabilizedplus
Make rs1479355(C;C)
Make rs1479355(C;T)
Make rs1479355(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position160109594
is asnp
is mentioned by
dbSNPrs1479355
ebirs1479355
HLIrs1479355
Exacrs1479355
Varsomers1479355
Maprs1479355
PheGenIrs1479355
hapmaprs1479355
1000 genomesrs1479355
hgdprs1479355
ensemblrs1479355
gopubmedrs1479355
geneviewrs1479355
scholarrs1479355
googlers1479355
pharmgkbrs1479355
gwascentralrs1479355
openSNPrs1479355
23andMers1479355
23andMe allrs1479355
SNP Nexus

SNPshotrs1479355
SNPdbers1479355
MSV3drs1479355
GWAS Ctlgrs1479355
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25867398] Associations between genetic variants and the severity of metabolic syndrome in subjects with type 2 diabetes