rs796052088

Orientation

plus

Stabilized

plus

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

Make rs796052088(A;A)

Make rs796052088(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97598790

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs796052088
dbSNP (classic)	rs796052088
ClinGen	rs796052088
ebi	rs796052088
HLI	rs796052088
Exac	rs796052088
Gnomad	rs796052088
Varsome	rs796052088
LitVar	rs796052088
Map	rs796052088
PheGenI	rs796052088
Biobank	rs796052088
1000 genomes	rs796052088
hgdp	rs796052088
ensembl	rs796052088
geneview	rs796052088
scholar	rs796052088
google	rs796052088
pharmgkb	rs796052088
gwascentral	rs796052088
openSNP	rs796052088
23andMe	rs796052088
SNPshot	rs796052088
SNPdbe	rs796052088
MSV3d	rs796052088
GWAS Ctlg	rs796052088

Max Magnitude

0

ClinVar
Risk	rs796052088(A;A)
Alt	rs796052088(A;A)
Reference	Rs796052088(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99358547G>A
CLNSRC
CLNACC	RCV000186487.1,