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rs121912727

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912727(A;A)
Make rs121912727(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836073
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912727
ebirs121912727
HLIrs121912727
Exacrs121912727
Varsomers121912727
Maprs121912727
PheGenIrs121912727
hapmaprs121912727
1000 genomesrs121912727
hgdprs121912727
ensemblrs121912727
gopubmedrs121912727
geneviewrs121912727
scholarrs121912727
googlers121912727
pharmgkbrs121912727
gwascentralrs121912727
openSNPrs121912727
23andMers121912727
23andMe allrs121912727
SNP Nexus

SNPshotrs121912727
SNPdbers121912727
MSV3drs121912727
GWAS Ctlgrs121912727
Max Magnitude0
OMIM107680
Desc
Variant0022
Relatedalso
ClinVar
Risk rs121912727(A;A)
Alt rs121912727(A;A)
Reference rs121912727(T;T)
Significance Pathogenic
Disease Apolipoprotein A-I deficiency
Variation info
Gene APOA1-AS APOA1
CLNDBN Apolipoprotein A-I deficiency
Reversed 1
HGVS NC_000011.9:g.116706789A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019522.27,