rs796052089

Orientation

plus

Stabilized

plus

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

Make rs796052089(A;T)

Make rs796052089(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

97598871

Gene

HOGA1

is a	snp
is	mentioned by
dbSNP	rs796052089
dbSNP (classic)	rs796052089
ClinGen	rs796052089
ebi	rs796052089
HLI	rs796052089
Exac	rs796052089
Gnomad	rs796052089
Varsome	rs796052089
LitVar	rs796052089
Map	rs796052089
PheGenI	rs796052089
Biobank	rs796052089
1000 genomes	rs796052089
hgdp	rs796052089
ensembl	rs796052089
geneview	rs796052089
scholar	rs796052089
google	rs796052089
pharmgkb	rs796052089
gwascentral	rs796052089
openSNP	rs796052089
23andMe	rs796052089
SNPshot	rs796052089
SNPdbe	rs796052089
MSV3d	rs796052089
GWAS Ctlg	rs796052089

Max Magnitude

0

ClinVar
Risk	rs796052089(T;T)
Alt	rs796052089(T;T)
Reference	Rs796052089(A;A)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	HOGA1
CLNDBN	Primary hyperoxaluria, type III
Reversed	0
HGVS	NC_000010.10:g.99358628A>T
CLNSRC
CLNACC	RCV000186488.1,