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rs10498712

From SNPedia

Orientationminus
Stabilizedminus
Make rs10498712(C;C)
Make rs10498712(C;T)
Make rs10498712(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position22743174
is asnp
is mentioned by
dbSNPrs10498712
ebirs10498712
HLIrs10498712
Exacrs10498712
Varsomers10498712
Maprs10498712
PheGenIrs10498712
hapmaprs10498712
1000 genomesrs10498712
hgdprs10498712
ensemblrs10498712
gopubmedrs10498712
geneviewrs10498712
scholarrs10498712
googlers10498712
pharmgkbrs10498712
gwascentralrs10498712
openSNPrs10498712
23andMers10498712
23andMe allrs10498712
SNP Nexus

SNPshotrs10498712
SNPdbers10498712
MSV3drs10498712
GWAS Ctlgrs10498712
GMAF0.2778
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele G
P-val 0.000009
Odds Ratio 0.23 [NR] mg/dL increase

HDL cholesterol levels being the quantitative trait associated with in [PMID 19197348OA-icon.png]


GET Evidence
rs10498712
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary