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rs387906413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906413(-;-)
Make rs387906413(-;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position104830993
GeneABCA1
is asnp
is mentioned by
dbSNPrs387906413
ebirs387906413
HLIrs387906413
Exacrs387906413
Varsomers387906413
Maprs387906413
PheGenIrs387906413
hapmaprs387906413
1000 genomesrs387906413
hgdprs387906413
ensemblrs387906413
gopubmedrs387906413
geneviewrs387906413
scholarrs387906413
googlers387906413
pharmgkbrs387906413
gwascentralrs387906413
openSNPrs387906413
23andMers387906413
23andMe allrs387906413
SNP Nexus

SNPshotrs387906413
SNPdbers387906413
MSV3drs387906413
GWAS Ctlgrs387906413
Max Magnitude0
ClinVar
Risk rs387906413(;)
Alt rs387906413(;)
Reference rs387906413(G;G)
Significance Pathogenic
Disease Tangier disease
Variation info
Gene ABCA1
CLNDBN Tangier disease
Reversed 1
HGVS NC_000009.11:g.107593274delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000010095.5,