rs387907296

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs387907296(A;T)

Make rs387907296(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

133973807

Gene

SLCO2A1

is a	snp
is	mentioned by
dbSNP	rs387907296
dbSNP (classic)	rs387907296
ClinGen	rs387907296
ebi	rs387907296
HLI	rs387907296
Exac	rs387907296
Gnomad	rs387907296
Varsome	rs387907296
LitVar	rs387907296
Map	rs387907296
PheGenI	rs387907296
Biobank	rs387907296
1000 genomes	rs387907296
hgdp	rs387907296
ensembl	rs387907296
geneview	rs387907296
scholar	rs387907296
google	rs387907296
pharmgkb	rs387907296
gwascentral	rs387907296
openSNP	rs387907296
23andMe	rs387907296
SNPshot	rs387907296
SNPdbe	rs387907296
MSV3d	rs387907296
GWAS Ctlg	rs387907296

Max Magnitude

0

ClinVar
Risk	rs387907296(G;G) rs387907296(T;T)
Alt	rs387907296(G;G) rs387907296(T;T)
Reference	Rs387907296(A;A)
Significance	Pathogenic
Disease	Primary hypertrophic osteoarthropathy
Variation	info
Gene	SLCO2A1
CLNDBN	Primary hypertrophic osteoarthropathy, autosomal recessive 2
Reversed	1
HGVS	NC_000003.11:g.133692651T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030781.2,