Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AACTC;AACTC) 0 common in clinvar
(CTCAA;CTCAA) 0 common in clinvar
Make rs398122988(-;-)
Make rs398122988(-;CTCAA)
ReferenceGRCh38 38.1/141
Chromosome1
Position62597929
GeneANGPTL3, DOCK7
is asnp
is mentioned by
dbSNPrs398122988
ebirs398122988
HLIrs398122988
Exacrs398122988
Varsomers398122988
Maprs398122988
PheGenIrs398122988
hapmaprs398122988
1000 genomesrs398122988
hgdprs398122988
ensemblrs398122988
gopubmedrs398122988
geneviewrs398122988
scholarrs398122988
googlers398122988
pharmgkbrs398122988
gwascentralrs398122988
openSNPrs398122988
23andMers398122988
23andMe allrs398122988
SNP Nexus

SNPshotrs398122988
SNPdbers398122988
MSV3drs398122988
GWAS Ctlgrs398122988
Max Magnitude0
ClinVar
Risk rs398122988(;)
Alt rs398122988(;)
Reference rs398122988(AACTC;AACTC)
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,