rs796052082

Orientation

plus

Stabilized

plus

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

Make rs796052082(-;-)

Make rs796052082(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37430606

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs796052082
dbSNP (classic)	rs796052082
ClinGen	rs796052082
ebi	rs796052082
HLI	rs796052082
Exac	rs796052082
Gnomad	rs796052082
Varsome	rs796052082
LitVar	rs796052082
Map	rs796052082
PheGenI	rs796052082
Biobank	rs796052082
1000 genomes	rs796052082
hgdp	rs796052082
ensembl	rs796052082
geneview	rs796052082
scholar	rs796052082
google	rs796052082
pharmgkb	rs796052082
gwascentral	rs796052082
openSNP	rs796052082
23andMe	rs796052082
SNPshot	rs796052082
SNPdbe	rs796052082
MSV3d	rs796052082
GWAS Ctlg	rs796052082

Max Magnitude

0

ClinVar
Risk	rs796052082(-;-)
Alt	rs796052082(-;-)
Reference	Rs796052082(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37430603delC
CLNSRC
CLNACC	RCV000186460.1,