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rs28931575

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28931575(C;C)
Make rs28931575(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836271
GeneAPOA1
is asnp
is mentioned by
dbSNPrs28931575
ebirs28931575
HLIrs28931575
Exacrs28931575
Varsomers28931575
Maprs28931575
PheGenIrs28931575
hapmaprs28931575
1000 genomesrs28931575
hgdprs28931575
ensemblrs28931575
gopubmedrs28931575
geneviewrs28931575
scholarrs28931575
googlers28931575
pharmgkbrs28931575
gwascentralrs28931575
openSNPrs28931575
23andMers28931575
23andMe allrs28931575
SNP Nexus

SNPshotrs28931575
SNPdbers28931575
MSV3drs28931575
GWAS Ctlgrs28931575
Max Magnitude0
OMIM107680
DescAMYLOIDOSIS, CARDIAC AND CUTANEOUS
Variant0024
Relatedalso


ClinVar
Risk rs28931575(C;C)
Alt rs28931575(C;C)
Reference rs28931575(T;T)
Significance Pathogenic
Disease Amyloidosis
Variation info
Gene APOA1-AS APOA1
CLNDBN Amyloidosis, cardiac and cutaneous
Reversed 1
HGVS NC_000011.9:g.116706987A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019524.27,