rs776813259

Orientation

plus

Stabilized

plus

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

Make rs776813259(A;A)

Make rs776813259(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

133935781

Gene

SLCO2A1

is a	snp
is	mentioned by
dbSNP	rs776813259
dbSNP (classic)	rs776813259
ClinGen	rs776813259
ebi	rs776813259
HLI	rs776813259
Exac	rs776813259
Gnomad	rs776813259
Varsome	rs776813259
LitVar	rs776813259
Map	rs776813259
PheGenI	rs776813259
Biobank	rs776813259
1000 genomes	rs776813259
hgdp	rs776813259
ensembl	rs776813259
geneview	rs776813259
scholar	rs776813259
google	rs776813259
pharmgkb	rs776813259
gwascentral	rs776813259
openSNP	rs776813259
23andMe	rs776813259
SNPshot	rs776813259
SNPdbe	rs776813259
MSV3d	rs776813259
GWAS Ctlg	rs776813259

Max Magnitude

0

ClinVar
Risk	rs776813259(A;A)
Alt	rs776813259(A;A)
Reference	Rs776813259(G;G)
Significance	Pathogenic
Disease	Primary hypertrophic osteoarthropathy
Variation	info
Gene	SLCO2A1
CLNDBN	Primary hypertrophic osteoarthropathy, autosomal recessive 2
Reversed	0
HGVS	NC_000003.11:g.133654625G>A
CLNSRC
CLNACC	RCV000490280.1,