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rs387907297

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907297(G;T)
Make rs387907297(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position133973750
GeneSLCO2A1
is asnp
is mentioned by
dbSNPrs387907297
ebirs387907297
HLIrs387907297
Exacrs387907297
Varsomers387907297
Maprs387907297
PheGenIrs387907297
hapmaprs387907297
1000 genomesrs387907297
hgdprs387907297
ensemblrs387907297
gopubmedrs387907297
geneviewrs387907297
scholarrs387907297
googlers387907297
pharmgkbrs387907297
gwascentralrs387907297
openSNPrs387907297
23andMers387907297
23andMe allrs387907297
SNP Nexus

SNPshotrs387907297
SNPdbers387907297
MSV3drs387907297
GWAS Ctlgrs387907297
Max Magnitude0
ClinVar
Risk rs387907297(A,T;A,T)
Alt rs387907297(A,T;A,T)
Reference rs387907297(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.133692594C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030782.3,