rs1057516299

Orientation

plus

Stabilized

plus

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

Make rs1057516299(-;-)

Make rs1057516299(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37426654

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516299
dbSNP (classic)	rs1057516299
ClinGen	rs1057516299
ebi	rs1057516299
HLI	rs1057516299
Exac	rs1057516299
Gnomad	rs1057516299
Varsome	rs1057516299
LitVar	rs1057516299
Map	rs1057516299
PheGenI	rs1057516299
Biobank	rs1057516299
1000 genomes	rs1057516299
hgdp	rs1057516299
ensembl	rs1057516299
geneview	rs1057516299
scholar	rs1057516299
google	rs1057516299
pharmgkb	rs1057516299
gwascentral	rs1057516299
openSNP	rs1057516299
23andMe	rs1057516299
SNPshot	rs1057516299
SNPdbe	rs1057516299
MSV3d	rs1057516299
GWAS Ctlg	rs1057516299

Max Magnitude

0

ClinVar
Risk	rs1057516299(-;-)
Alt	rs1057516299(-;-)
Reference	Rs1057516299(A;A)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37426651delA
CLNSRC
CLNACC	RCV000410867.1,