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rs4844614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs4844614(G;T)
Make rs4844614(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position207701830
GeneCR1L
is asnp
is mentioned by
dbSNPrs4844614
ebirs4844614
HLIrs4844614
Exacrs4844614
Varsomers4844614
Maprs4844614
PheGenIrs4844614
hapmaprs4844614
1000 genomesrs4844614
hgdprs4844614
ensemblrs4844614
gopubmedrs4844614
geneviewrs4844614
scholarrs4844614
googlers4844614
pharmgkbrs4844614
gwascentralrs4844614
openSNPrs4844614
23andMers4844614
23andMe allrs4844614
SNP Nexus

SNPshotrs4844614
SNPdbers4844614
MSV3drs4844614
GWAS Ctlgrs4844614
GMAF0.3264
Max Magnitude0
? (G;G) (G;T) (T;T) 28
per the 23andMe blog, the minor allele of this SNP (T) was associated with increased LDL cholesterol
SNP Rarer allele LDL HDL TG
rs6544713 T +
rs2650000 A +
rs471364 C -
rs1800961 T -
rs7679 C - +
rs2967605 T -
rs2409722 T -
rs10903129 A - - -
rs6756629 A - + -
rs12670798 C + + +
rs7395662 A - + +
rs174570 T - - +
rs2271293 A - + -
rs2624265 C +
rs2167079 T +
rs9891572 T +
rs4844614 T +
rs5031002 G +
GWAS snp
PMID [PMID 19060910OA-icon.png]
Trait LDL cholesterol
Title Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Risk Allele A
P-val 2E-7
Odds Ratio 0.10 [0.06-0.14] mmol/l increase



GET Evidence
rs4844614
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.365079
summary