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rs562574661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
Make rs562574661(-;-)
Make rs562574661(-;CTG)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position21001940
GeneAPOB
is asnp
is mentioned by
dbSNPrs562574661
dbSNP (classic)rs562574661
ClinGenrs562574661
ebirs562574661
HLIrs562574661
Exacrs562574661
Gnomadrs562574661
Varsomers562574661
LitVarrs562574661
Maprs562574661
PheGenIrs562574661
Biobankrs562574661
1000 genomesrs562574661
hgdprs562574661
ensemblrs562574661
geneviewrs562574661
scholarrs562574661
googlers562574661
pharmgkbrs562574661
gwascentralrs562574661
openSNPrs562574661
23andMers562574661
23andMe allrs562574661
SNPshotrs562574661
SNPdbers562574661
MSV3drs562574661
GWAS Ctlgrs562574661
Max Magnitude0
ClinVar
Risk rs562574661(-;-)
Alt rs562574661(-;-)
Reference Rs562574661(CTG;CTG)
Significance Other
Disease Familial hypercholesterolemia
Variation info
Gene APOB
CLNDBN Familial hypercholesterolemia
Reversed 0
HGVS NC_000002.11:g.21224812_21224814delCTG
CLNSRC Instituto Nacional de Saúde Doutor Ricardo Jorge The University of Western Ontario
CLNACC RCV000256307.1,