rs796052079

Orientation

plus

Stabilized

plus

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

Make rs796052079(A;A)

Make rs796052079(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37432016

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs796052079
dbSNP (classic)	rs796052079
ClinGen	rs796052079
ebi	rs796052079
HLI	rs796052079
Exac	rs796052079
Gnomad	rs796052079
Varsome	rs796052079
LitVar	rs796052079
Map	rs796052079
PheGenI	rs796052079
Biobank	rs796052079
1000 genomes	rs796052079
hgdp	rs796052079
ensembl	rs796052079
geneview	rs796052079
scholar	rs796052079
google	rs796052079
pharmgkb	rs796052079
gwascentral	rs796052079
openSNP	rs796052079
23andMe	rs796052079
SNPshot	rs796052079
SNPdbe	rs796052079
MSV3d	rs796052079
GWAS Ctlg	rs796052079

Max Magnitude

0

ClinVar
Risk	rs796052079(A;A)
Alt	rs796052079(A;A)
Reference	Rs796052079(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37432013T>A
CLNSRC
CLNACC	RCV000186443.1,