rs796052081

Orientation

plus

Stabilized

plus

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

Make rs796052081(-;-)

Make rs796052081(-;AGT)

Make rs796052081(AGT;AGT)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37426536

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs796052081
dbSNP (classic)	rs796052081
ClinGen	rs796052081
ebi	rs796052081
HLI	rs796052081
Exac	rs796052081
Gnomad	rs796052081
Varsome	rs796052081
LitVar	rs796052081
Map	rs796052081
PheGenI	rs796052081
Biobank	rs796052081
1000 genomes	rs796052081
hgdp	rs796052081
ensembl	rs796052081
geneview	rs796052081
scholar	rs796052081
google	rs796052081
pharmgkb	rs796052081
gwascentral	rs796052081
openSNP	rs796052081
23andMe	rs796052081
SNPshot	rs796052081
SNPdbe	rs796052081
MSV3d	rs796052081
GWAS Ctlg	rs796052081

Max Magnitude

0

ClinVar
Risk	rs796052081(-;-)
Alt	rs796052081(-;-)
Reference	Rs796052081(GTA;GTA)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37426533_37426535delAGT
CLNSRC
CLNACC	RCV000186454.1,