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rs1048886

From SNPedia

Orientationplus
Stabilizedplus
Make rs1048886(A;A)
Make rs1048886(A;G)
Make rs1048886(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position70579486
GeneC6orf57
is asnp
is mentioned by
dbSNPrs1048886
ebirs1048886
HLIrs1048886
Exacrs1048886
Varsomers1048886
Maprs1048886
PheGenIrs1048886
hapmaprs1048886
1000 genomesrs1048886
hgdprs1048886
ensemblrs1048886
gopubmedrs1048886
geneviewrs1048886
scholarrs1048886
googlers1048886
pharmgkbrs1048886
gwascentralrs1048886
openSNPrs1048886
23andMers1048886
23andMe allrs1048886
SNP Nexus

SNPshotrs1048886
SNPdbers1048886
MSV3drs1048886
GWAS Ctlgrs1048886
GMAF0.2048
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21490949OA-icon.png]
Trait
Title Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
Risk Allele G
P-val 3E-8
Odds Ratio 1.5400 [1.32-1.80]


GET Evidence
C6ORF57-Q46R
aa_change Gln46Arg
aa_change_short Q46R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.218349
summary