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rs137854494

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854494(C;C)
Make rs137854494(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position104806276
GeneABCA1
is asnp
is mentioned by
dbSNPrs137854494
ebirs137854494
HLIrs137854494
Exacrs137854494
Varsomers137854494
Maprs137854494
PheGenIrs137854494
hapmaprs137854494
1000 genomesrs137854494
hgdprs137854494
ensemblrs137854494
gopubmedrs137854494
geneviewrs137854494
scholarrs137854494
googlers137854494
pharmgkbrs137854494
gwascentralrs137854494
openSNPrs137854494
23andMers137854494
23andMe allrs137854494
SNP Nexus

SNPshotrs137854494
SNPdbers137854494
MSV3drs137854494
GWAS Ctlgrs137854494
Max Magnitude0
OMIM600046
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137854494(C;C)
Alt rs137854494(C;C)
Reference rs137854494(T;T)
Significance Pathogenic
Disease Tangier disease
Variation info
Gene ABCA1
CLNDBN Tangier disease
Reversed 1
HGVS NC_000009.11:g.107568557A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010091.4,