rs796052080

Orientation

plus

Stabilized

plus

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

Make rs796052080(-;-)

Make rs796052080(-;CC)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37424832

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs796052080
dbSNP (classic)	rs796052080
ClinGen	rs796052080
ebi	rs796052080
HLI	rs796052080
Exac	rs796052080
Gnomad	rs796052080
Varsome	rs796052080
LitVar	rs796052080
Map	rs796052080
PheGenI	rs796052080
Biobank	rs796052080
1000 genomes	rs796052080
hgdp	rs796052080
ensembl	rs796052080
geneview	rs796052080
scholar	rs796052080
google	rs796052080
pharmgkb	rs796052080
gwascentral	rs796052080
openSNP	rs796052080
23andMe	rs796052080
SNPshot	rs796052080
SNPdbe	rs796052080
MSV3d	rs796052080
GWAS Ctlg	rs796052080

Max Magnitude

0

ClinVar
Risk	rs796052080(-;-)
Alt	rs796052080(-;-)
Reference	Rs796052080(CC;CC)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37424829_37424830delCC
CLNSRC
CLNACC	RCV000186453.1,