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rs7396835

From SNPedia

Orientationplus
Stabilizedplus
Make rs7396835(C;C)
Make rs7396835(C;T)
Make rs7396835(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116813312
is asnp
is mentioned by
dbSNPrs7396835
ebirs7396835
HLIrs7396835
Exacrs7396835
Varsomers7396835
Maprs7396835
PheGenIrs7396835
hapmaprs7396835
1000 genomesrs7396835
hgdprs7396835
ensemblrs7396835
gopubmedrs7396835
geneviewrs7396835
scholarrs7396835
googlers7396835
pharmgkbrs7396835
gwascentralrs7396835
openSNPrs7396835
23andMers7396835
23andMe allrs7396835
SNP Nexus

SNPshotrs7396835
SNPdbers7396835
MSV3drs7396835
GWAS Ctlgrs7396835
GMAF0.208
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 T
P-val 1E-9
Odds Ratio 0.23 [NR] mg/dL increase

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


GET Evidence
rs7396835
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.796875
summary