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rs121912728

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912728(C;C)
Make rs121912728(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836022
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912728
ebirs121912728
HLIrs121912728
Exacrs121912728
Varsomers121912728
Maprs121912728
PheGenIrs121912728
hapmaprs121912728
1000 genomesrs121912728
hgdprs121912728
ensemblrs121912728
gopubmedrs121912728
geneviewrs121912728
scholarrs121912728
googlers121912728
pharmgkbrs121912728
gwascentralrs121912728
openSNPrs121912728
23andMers121912728
23andMe allrs121912728
SNP Nexus

SNPshotrs121912728
SNPdbers121912728
MSV3drs121912728
GWAS Ctlgrs121912728
Max Magnitude0
OMIM107680
Desc
Variant0025
Relatedalso
ClinVar
Risk rs121912728(C;C)
Alt rs121912728(C;C)
Reference rs121912728(G;G)
Significance Pathogenic
Disease Amyloidosis
Variation info
Gene APOA1
CLNDBN Amyloidosis, cardiac and cutaneous
Reversed 1
HGVS NC_000011.9:g.116706738C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019525.26,