rs796052078

Orientation

plus

Stabilized

plus

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

Make rs796052078(G;T)

Make rs796052078(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37425994

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs796052078
dbSNP (classic)	rs796052078
ClinGen	rs796052078
ebi	rs796052078
HLI	rs796052078
Exac	rs796052078
Gnomad	rs796052078
Varsome	rs796052078
LitVar	rs796052078
Map	rs796052078
PheGenI	rs796052078
Biobank	rs796052078
1000 genomes	rs796052078
hgdp	rs796052078
ensembl	rs796052078
geneview	rs796052078
scholar	rs796052078
google	rs796052078
pharmgkb	rs796052078
gwascentral	rs796052078
openSNP	rs796052078
23andMe	rs796052078
SNPshot	rs796052078
SNPdbe	rs796052078
MSV3d	rs796052078
GWAS Ctlg	rs796052078

Max Magnitude

0

ClinVar
Risk	rs796052078(A;A) rs796052078(T;T)
Alt	rs796052078(A;A) rs796052078(T;T)
Reference	Rs796052078(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37425991G>T
CLNSRC
CLNACC	RCV000186440.1,