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rs17240441

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGGCGCTGC;TGGCGCTGC) 0 common in clinvar
Make rs17240441(-;-)
Make rs17240441(-;CGTCGCGGT)
Make rs17240441(CGTCGCGGT;CGTCGCGGT)
ReferenceGRCh38 38.1/142
Chromosome2
Position21043903
GeneAPOB, LOC101929195
is asnp
is mentioned by
dbSNPrs17240441
ClinGenrs17240441
ebirs17240441
HLIrs17240441
Exacrs17240441
Varsomers17240441
Maprs17240441
PheGenIrs17240441
hapmaprs17240441
1000 genomesrs17240441
hgdprs17240441
ensemblrs17240441
gopubmedrs17240441
geneviewrs17240441
scholarrs17240441
googlers17240441
pharmgkbrs17240441
gwascentralrs17240441
openSNPrs17240441
23andMers17240441
23andMe allrs17240441
SNP Nexus

SNPshotrs17240441
SNPdbers17240441
MSV3drs17240441
GWAS Ctlgrs17240441
Max Magnitude0

[PMID 25793007OA-icon.png] The APOB insertion/deletion polymorphism (rs17240441) influences postprandial lipaemia in healthy adults

ClinVar
Risk rs17240441(-;-)
Alt rs17240441(-;-)
Reference Rs17240441(TGGCGCTGC;TGGCGCTGC)
Significance Other
Disease not specified Familial hypercholesterolemia
Variation info
Gene LOC101929195 APOB
CLNDBN not specified Familial hypercholesterolemia
Reversed 1
HGVS NC_000002.11:g.21266775_21266783delGCAGCGCCA
CLNSRC Instituto Nacional de Saúde Doutor Ricardo Jorge
CLNACC RCV000251913.1, RCV000256231.2,