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rs387906571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906571(C;C)
Make rs387906571(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836094
GeneAPOA1
is asnp
is mentioned by
dbSNPrs387906571
ebirs387906571
HLIrs387906571
Exacrs387906571
Varsomers387906571
Maprs387906571
PheGenIrs387906571
hapmaprs387906571
1000 genomesrs387906571
hgdprs387906571
ensemblrs387906571
gopubmedrs387906571
geneviewrs387906571
scholarrs387906571
googlers387906571
pharmgkbrs387906571
gwascentralrs387906571
openSNPrs387906571
23andMers387906571
23andMe allrs387906571
SNP Nexus

SNPshotrs387906571
SNPdbers387906571
MSV3drs387906571
GWAS Ctlgrs387906571
Max Magnitude0
ClinVar
Risk rs387906571(C;C)
Alt rs387906571(C;C)
Reference rs387906571(G;G)
Significance Pathogenic
Disease Amyloidosis
Variation info
Gene APOA1-AS APOA1
CLNDBN Amyloidosis, cardiac and cutaneous
Reversed 1
HGVS NC_000011.9:g.116706810C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019525.27,