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rs121912722

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912722(C;G)
Make rs121912722(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116836046
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912722
ebirs121912722
HLIrs121912722
Exacrs121912722
Varsomers121912722
Maprs121912722
PheGenIrs121912722
hapmaprs121912722
1000 genomesrs121912722
hgdprs121912722
ensemblrs121912722
gopubmedrs121912722
geneviewrs121912722
scholarrs121912722
googlers121912722
pharmgkbrs121912722
gwascentralrs121912722
openSNPrs121912722
23andMers121912722
23andMe allrs121912722
SNP Nexus

SNPshotrs121912722
SNPdbers121912722
MSV3drs121912722
GWAS Ctlgrs121912722
Max Magnitude0
OMIM107680
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121912722(G;G)
Alt rs121912722(G;G)
Reference rs121912722(C;C)
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.116706762G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019505.27,