rs1057516292

Orientation

plus

Stabilized

plus

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

Make rs1057516292(-;-)

Make rs1057516292(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37429835

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516292
dbSNP (classic)	rs1057516292
ClinGen	rs1057516292
ebi	rs1057516292
HLI	rs1057516292
Exac	rs1057516292
Gnomad	rs1057516292
Varsome	rs1057516292
LitVar	rs1057516292
Map	rs1057516292
PheGenI	rs1057516292
Biobank	rs1057516292
1000 genomes	rs1057516292
hgdp	rs1057516292
ensembl	rs1057516292
geneview	rs1057516292
scholar	rs1057516292
google	rs1057516292
pharmgkb	rs1057516292
gwascentral	rs1057516292
openSNP	rs1057516292
23andMe	rs1057516292
SNPshot	rs1057516292
SNPdbe	rs1057516292
MSV3d	rs1057516292
GWAS Ctlg	rs1057516292

Max Magnitude

0

ClinVar
Risk	rs1057516292(-;-)
Alt	rs1057516292(-;-)
Reference	Rs1057516292(T;T)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37429832delT
CLNSRC
CLNACC	RCV000409935.1,