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rs387906806

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906806(A;A)
Make rs387906806(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position133951305
GeneSLCO2A1
is asnp
is mentioned by
dbSNPrs387906806
ebirs387906806
HLIrs387906806
Exacrs387906806
Varsomers387906806
Maprs387906806
PheGenIrs387906806
hapmaprs387906806
1000 genomesrs387906806
hgdprs387906806
ensemblrs387906806
gopubmedrs387906806
geneviewrs387906806
scholarrs387906806
googlers387906806
pharmgkbrs387906806
gwascentralrs387906806
openSNPrs387906806
23andMers387906806
23andMe allrs387906806
SNP Nexus

SNPshotrs387906806
SNPdbers387906806
MSV3drs387906806
GWAS Ctlgrs387906806
Max Magnitude0
ClinVar
Risk rs387906806(A;A)
Alt rs387906806(A;A)
Reference rs387906806(G;G)
Significance Pathogenic
Disease Primary hypertrophic osteoarthropathy
Variation info
Gene SLCO2A1
CLNDBN Primary hypertrophic osteoarthropathy, autosomal recessive 2
Reversed 1
HGVS NC_000003.11:g.133670149C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023105.2,