rs387907297

Orientation

minus

Stabilized

minus

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

Make rs387907297(G;T)

Make rs387907297(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

133973750

Gene

SLCO2A1

is a	snp
is	mentioned by
dbSNP	rs387907297
dbSNP (classic)	rs387907297
ClinGen	rs387907297
ebi	rs387907297
HLI	rs387907297
Exac	rs387907297
Gnomad	rs387907297
Varsome	rs387907297
LitVar	rs387907297
Map	rs387907297
PheGenI	rs387907297
Biobank	rs387907297
1000 genomes	rs387907297
hgdp	rs387907297
ensembl	rs387907297
geneview	rs387907297
scholar	rs387907297
google	rs387907297
pharmgkb	rs387907297
gwascentral	rs387907297
openSNP	rs387907297
23andMe	rs387907297
SNPshot	rs387907297
SNPdbe	rs387907297
MSV3d	rs387907297
GWAS Ctlg	rs387907297

Max Magnitude

0

ClinVar
Risk	rs387907297(A;A) rs387907297(T;T)
Alt	rs387907297(A;A) rs387907297(T;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,