rs387906412

Orientation

minus

Stabilized

minus

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

Make rs387906412(-;-)

Make rs387906412(-;CTT)

Reference

GRCh38 38.1/141

Chromosome

9

Position

104828949

Gene

ABCA1

is a	snp
is	mentioned by
dbSNP	rs387906412
dbSNP (classic)	rs387906412
ClinGen	rs387906412
ebi	rs387906412
HLI	rs387906412
Exac	rs387906412
Gnomad	rs387906412
Varsome	rs387906412
LitVar	rs387906412
Map	rs387906412
PheGenI	rs387906412
Biobank	rs387906412
1000 genomes	rs387906412
hgdp	rs387906412
ensembl	rs387906412
geneview	rs387906412
scholar	rs387906412
google	rs387906412
pharmgkb	rs387906412
gwascentral	rs387906412
openSNP	rs387906412
23andMe	rs387906412
SNPshot	rs387906412
SNPdbe	rs387906412
MSV3d	rs387906412
GWAS Ctlg	rs387906412

Max Magnitude

0

ClinVar
Risk	rs387906412(-;-)
Alt	rs387906412(-;-)
Reference	Rs387906412(CTT;CTT)
Significance	Pathogenic
Disease	Familial hypoalphalipoproteinemia
Variation	info
Gene	ABCA1
CLNDBN	Familial hypoalphalipoproteinemia
Reversed	1
HGVS	NC_000009.11:g.107591230_107591232delAAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010094.5,