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rs796051872

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796051872(C;C)
Make rs796051872(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position104816142
GeneABCA1
is asnp
is mentioned by
dbSNPrs796051872
ebirs796051872
HLIrs796051872
Exacrs796051872
Varsomers796051872
Maprs796051872
PheGenIrs796051872
hapmaprs796051872
1000 genomesrs796051872
hgdprs796051872
ensemblrs796051872
gopubmedrs796051872
geneviewrs796051872
scholarrs796051872
googlers796051872
pharmgkbrs796051872
gwascentralrs796051872
openSNPrs796051872
23andMers796051872
23andMe allrs796051872
SNP Nexus

SNPshotrs796051872
SNPdbers796051872
MSV3drs796051872
GWAS Ctlgrs796051872
Max Magnitude0
ClinVar
Risk rs796051872(C;C)
Alt rs796051872(C;C)
Reference rs796051872(G;G)
Significance Pathogenic
Disease Tangier disease
Variation info
Gene ABCA1
CLNDBN Tangier disease
Reversed 1
HGVS NC_000009.11:g.107578423C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010092.4,