rs1057516831

Orientation

plus

Stabilized

plus

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

Make rs1057516831(-;-)

Make rs1057516831(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37436749

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516831
dbSNP (classic)	rs1057516831
ClinGen	rs1057516831
ebi	rs1057516831
HLI	rs1057516831
Exac	rs1057516831
Gnomad	rs1057516831
Varsome	rs1057516831
LitVar	rs1057516831
Map	rs1057516831
PheGenI	rs1057516831
Biobank	rs1057516831
1000 genomes	rs1057516831
hgdp	rs1057516831
ensembl	rs1057516831
geneview	rs1057516831
scholar	rs1057516831
google	rs1057516831
pharmgkb	rs1057516831
gwascentral	rs1057516831
openSNP	rs1057516831
23andMe	rs1057516831
SNPshot	rs1057516831
SNPdbe	rs1057516831
MSV3d	rs1057516831
GWAS Ctlg	rs1057516831

Max Magnitude

0

ClinVar
Risk	rs1057516831(-;-)
Alt	rs1057516831(-;-)
Reference	Rs1057516831(A;A)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37436746delA
CLNSRC
CLNACC	RCV000409992.1,