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rs387906390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs387906390(AAG;CTT)
Make rs387906390(CTT;CTT)
ReferenceGRCh38 38.1/141
Chromosome13
Position103052619
GeneSLC10A2
is asnp
is mentioned by
dbSNPrs387906390
ebirs387906390
HLIrs387906390
Exacrs387906390
Varsomers387906390
Maprs387906390
PheGenIrs387906390
hapmaprs387906390
1000 genomesrs387906390
hgdprs387906390
ensemblrs387906390
gopubmedrs387906390
geneviewrs387906390
scholarrs387906390
googlers387906390
pharmgkbrs387906390
gwascentralrs387906390
openSNPrs387906390
23andMers387906390
23andMe allrs387906390
SNP Nexus

SNPshotrs387906390
SNPdbers387906390
MSV3drs387906390
GWAS Ctlgrs387906390
Max Magnitude0
ClinVar
Risk rs387906390(CTT;CTT)
Alt rs387906390(CTT;CTT)
Reference rs387906390(AAG;AAG)
Significance Pathogenic
Disease Bile acid malabsorption
Variation info
Gene SLC10A2
CLNDBN Bile acid malabsorption, primary
Reversed 1
HGVS NC_000013.10:g.103704969_103704971delCTTinsAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000008725.3,