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rs12753193

From SNPedia

Orientationplus
Stabilizedplus
Make rs12753193(A;A)
Make rs12753193(A;G)
Make rs12753193(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position65703996
is asnp
is mentioned by
dbSNPrs12753193
ebirs12753193
HLIrs12753193
Exacrs12753193
Varsomers12753193
Maprs12753193
PheGenIrs12753193
hapmaprs12753193
1000 genomesrs12753193
hgdprs12753193
ensemblrs12753193
gopubmedrs12753193
geneviewrs12753193
scholarrs12753193
googlers12753193
pharmgkbrs12753193
gwascentralrs12753193
openSNPrs12753193
23andMers12753193
23andMe allrs12753193
SNP Nexus

SNPshotrs12753193
SNPdbers12753193
MSV3drs12753193
GWAS Ctlgrs12753193
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19060910OA-icon.png]
Trait Other metabolic traits
Title Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Risk Allele G
P-val 4E-7
Odds Ratio 0.13 [-0.02-0.27] mmol/l decrease



[PMID 20585554OA-icon.png] On the use of variance per genotype as a tool to identify quantitative trait interaction effects: a report from the Women's Genome Health Study


[PMID 18439548OA-icon.png] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.


[PMID 18439552OA-icon.png] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.


GET Evidence
rs12753193
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.554688
summary