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rs387906570

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906570(C;T)
Make rs387906570(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116837134
GeneAPOA1
is asnp
is mentioned by
dbSNPrs387906570
ebirs387906570
HLIrs387906570
Exacrs387906570
Varsomers387906570
Maprs387906570
PheGenIrs387906570
hapmaprs387906570
1000 genomesrs387906570
hgdprs387906570
ensemblrs387906570
gopubmedrs387906570
geneviewrs387906570
scholarrs387906570
googlers387906570
pharmgkbrs387906570
gwascentralrs387906570
openSNPrs387906570
23andMers387906570
23andMe allrs387906570
SNP Nexus

SNPshotrs387906570
SNPdbers387906570
MSV3drs387906570
GWAS Ctlgrs387906570
Max Magnitude0
ClinVar
Risk rs387906570(T;T)
Alt rs387906570(T;T)
Reference rs387906570(C;C)
Significance Pathogenic
Disease Tangier disease
Variation info
Gene APOA1-AS APOA1
CLNDBN Tangier disease
Reversed 1
HGVS NC_000011.9:g.116707850G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019517.27,