rs796051872

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs796051872(C;C)

Make rs796051872(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

104816142

Gene

ABCA1

is a	snp
is	mentioned by
dbSNP	rs796051872
dbSNP (classic)	rs796051872
ClinGen	rs796051872
ebi	rs796051872
HLI	rs796051872
Exac	rs796051872
Gnomad	rs796051872
Varsome	rs796051872
LitVar	rs796051872
Map	rs796051872
PheGenI	rs796051872
Biobank	rs796051872
1000 genomes	rs796051872
hgdp	rs796051872
ensembl	rs796051872
geneview	rs796051872
scholar	rs796051872
google	rs796051872
pharmgkb	rs796051872
gwascentral	rs796051872
openSNP	rs796051872
23andMe	rs796051872
SNPshot	rs796051872
SNPdbe	rs796051872
MSV3d	rs796051872
GWAS Ctlg	rs796051872

Max Magnitude

0

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,