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rs387906414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs387906414(-;-)
Make rs387906414(-;TC)
ReferenceGRCh38 38.1/141
Chromosome9
Position104818781
GeneABCA1
is asnp
is mentioned by
dbSNPrs387906414
dbSNP (classic)rs387906414
ClinGenrs387906414
ebirs387906414
HLIrs387906414
Exacrs387906414
Gnomadrs387906414
Varsomers387906414
LitVarrs387906414
Maprs387906414
PheGenIrs387906414
Biobankrs387906414
1000 genomesrs387906414
hgdprs387906414
ensemblrs387906414
geneviewrs387906414
scholarrs387906414
googlers387906414
pharmgkbrs387906414
gwascentralrs387906414
openSNPrs387906414
23andMers387906414
SNPshotrs387906414
SNPdbers387906414
MSV3drs387906414
GWAS Ctlgrs387906414
Max Magnitude0
ClinVar
Risk rs387906414(-;-)
Alt rs387906414(-;-)
Reference Rs387906414(TC;TC)
Significance Pathogenic
Disease Tangier disease
Variation info
Gene ABCA1
CLNDBN Tangier disease
Reversed 1
HGVS NC_000009.11:g.107581062_107581063delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010101.4,