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rs387906412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs387906412(-;-)
Make rs387906412(-;CTT)
ReferenceGRCh38 38.1/141
Chromosome9
Position104828949
GeneABCA1
is asnp
is mentioned by
dbSNPrs387906412
ebirs387906412
HLIrs387906412
Exacrs387906412
Varsomers387906412
Maprs387906412
PheGenIrs387906412
hapmaprs387906412
1000 genomesrs387906412
hgdprs387906412
ensemblrs387906412
gopubmedrs387906412
geneviewrs387906412
scholarrs387906412
googlers387906412
pharmgkbrs387906412
gwascentralrs387906412
openSNPrs387906412
23andMers387906412
23andMe allrs387906412
SNP Nexus

SNPshotrs387906412
SNPdbers387906412
MSV3drs387906412
GWAS Ctlgrs387906412
Max Magnitude0
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,