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rs2277862

From SNPedia

Orientationminus
Stabilizedminus
Make rs2277862(A;A)
Make rs2277862(A;G)
Make rs2277862(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position35564866
GeneFER1L4
is asnp
is mentioned by
dbSNPrs2277862
ebirs2277862
HLIrs2277862
Exacrs2277862
Varsomers2277862
Maprs2277862
PheGenIrs2277862
hapmaprs2277862
1000 genomesrs2277862
hgdprs2277862
ensemblrs2277862
gopubmedrs2277862
geneviewrs2277862
scholarrs2277862
googlers2277862
pharmgkbrs2277862
gwascentralrs2277862
openSNPrs2277862
23andMers2277862
23andMe allrs2277862
SNP Nexus

SNPshotrs2277862
SNPdbers2277862
MSV3drs2277862
GWAS Ctlgrs2277862
GMAF0.1474
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20686565OA-icon.png]
Trait
Title Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele T
P-val 4E-10
Odds Ratio 1.1900 None


GET Evidence
FER1L4-V665I
aa_change Val665Ile
aa_change_short V665I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.140625
summary



GWAS snp
PMID [PMID 24097068OA-icon.png]
Trait Cholesterol, total
Title Discovery and refinement of loci associated with lipid levels.
Risk Allele T
P-val 5E-11
Odds Ratio .04 [NR] unit decrease