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rs886039296

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039296(C;T)
Make rs886039296(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215018130
GeneABCA12
is asnp
is mentioned by
dbSNPrs886039296
dbSNP (classic)rs886039296
ClinGenrs886039296
ebirs886039296
HLIrs886039296
Exacrs886039296
Gnomadrs886039296
Varsomers886039296
LitVarrs886039296
Maprs886039296
PheGenIrs886039296
Biobankrs886039296
1000 genomesrs886039296
hgdprs886039296
ensemblrs886039296
geneviewrs886039296
scholarrs886039296
googlers886039296
pharmgkbrs886039296
gwascentralrs886039296
openSNPrs886039296
23andMers886039296
23andMe allrs886039296
SNPshotrs886039296
SNPdbers886039296
MSV3drs886039296
GWAS Ctlgrs886039296
Max Magnitude0
ClinVar
Risk rs886039296(T;T)
Alt rs886039296(T;T)
Reference Rs886039296(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.215882854G>A
CLNSRC
CLNACC RCV000255237.1,