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rs398122988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CTCAA) 5 Lowered risk (0.6x) of coronary artery disease
(AACTC;AACTC) 0 common in clinvar
(CTCAA;CTCAA) 0 common in clinvar


Make rs398122988(-;-)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position62597929
GeneANGPTL3, DOCK7
is asnp
is mentioned by
dbSNPrs398122988
dbSNP (classic)rs398122988
ClinGenrs398122988
ebirs398122988
HLIrs398122988
Exacrs398122988
Gnomadrs398122988
Varsomers398122988
LitVarrs398122988
Maprs398122988
PheGenIrs398122988
Biobankrs398122988
1000 genomesrs398122988
hgdprs398122988
ensemblrs398122988
geneviewrs398122988
scholarrs398122988
googlers398122988
pharmgkbrs398122988
gwascentralrs398122988
openSNPrs398122988
23andMers398122988
SNPshotrs398122988
SNPdbers398122988
MSV3drs398122988
GWAS Ctlgrs398122988
Merged fromRs569107562
Max Magnitude5

ANGPTL3, c.363_367delCTCAA (p.Asn121Lysfs)

ClinVar
Risk rs398122988(-;-) Rs398122988(AACTC;AACTC)
Alt rs398122988(-;-) Rs398122988(AACTC;AACTC)
Reference Rs398122988(CTCAA;CTCAA)
Significance Pathogenic
Disease Hypobetalipoproteinemia
Variation info
Gene DOCK7 ANGPTL3
CLNDBN Hypobetalipoproteinemia, familial, 2
Reversed 0
HGVS NC_000001.10:g.63063600_63063604delCTCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000077769.2,