rs796052087

Orientation

plus

Stabilized

plus

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

Make rs796052087(C;C)

Make rs796052087(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97611550

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs796052087
dbSNP (classic)	rs796052087
ClinGen	rs796052087
ebi	rs796052087
HLI	rs796052087
Exac	rs796052087
Gnomad	rs796052087
Varsome	rs796052087
LitVar	rs796052087
Map	rs796052087
PheGenI	rs796052087
Biobank	rs796052087
1000 genomes	rs796052087
hgdp	rs796052087
ensembl	rs796052087
geneview	rs796052087
scholar	rs796052087
google	rs796052087
pharmgkb	rs796052087
gwascentral	rs796052087
openSNP	rs796052087
23andMe	rs796052087
SNPshot	rs796052087
SNPdbe	rs796052087
MSV3d	rs796052087
GWAS Ctlg	rs796052087

Max Magnitude

0

ClinVar
Risk	rs796052087(C;C)
Alt	rs796052087(C;C)
Reference	Rs796052087(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99371307T>C
CLNSRC
CLNACC	RCV000186485.1,