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rs121912725

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912725(C;T)
Make rs121912725(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position116837035
GeneAPOA1
is asnp
is mentioned by
dbSNPrs121912725
ebirs121912725
HLIrs121912725
Exacrs121912725
Varsomers121912725
Maprs121912725
PheGenIrs121912725
hapmaprs121912725
1000 genomesrs121912725
hgdprs121912725
ensemblrs121912725
gopubmedrs121912725
geneviewrs121912725
scholarrs121912725
googlers121912725
pharmgkbrs121912725
gwascentralrs121912725
openSNPrs121912725
23andMers121912725
23andMe allrs121912725
SNP Nexus

SNPshotrs121912725
SNPdbers121912725
MSV3drs121912725
GWAS Ctlgrs121912725
Max Magnitude0
OMIM107680
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121912725(T;T)
Alt rs121912725(T;T)
Reference rs121912725(C;C)
Significance Pathogenic
Disease Xanthelasmas
Variation info
Gene APOA1-AS APOA1
CLNDBN Xanthelasmas, periorbital
Reversed 1
HGVS NC_000011.9:g.116707751G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019519.23,