rs1057517398

Orientation

plus

Stabilized

plus

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

Make rs1057517398(G;G)

Make rs1057517398(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37424977

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057517398
dbSNP (classic)	rs1057517398
ClinGen	rs1057517398
ebi	rs1057517398
HLI	rs1057517398
Exac	rs1057517398
Gnomad	rs1057517398
Varsome	rs1057517398
LitVar	rs1057517398
Map	rs1057517398
PheGenI	rs1057517398
Biobank	rs1057517398
1000 genomes	rs1057517398
hgdp	rs1057517398
ensembl	rs1057517398
geneview	rs1057517398
scholar	rs1057517398
google	rs1057517398
pharmgkb	rs1057517398
gwascentral	rs1057517398
openSNP	rs1057517398
23andMe	rs1057517398
SNPshot	rs1057517398
SNPdbe	rs1057517398
MSV3d	rs1057517398
GWAS Ctlg	rs1057517398

Max Magnitude

0

ClinVar
Risk	rs1057517398(G;G)
Alt	rs1057517398(G;G)
Reference	Rs1057517398(T;T)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37424974T>G
CLNSRC
CLNACC	RCV000410412.1,