rs1057516990

Orientation

plus

Stabilized

plus

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

Make rs1057516990(-;-)

Make rs1057516990(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37429753

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516990
dbSNP (classic)	rs1057516990
ClinGen	rs1057516990
ebi	rs1057516990
HLI	rs1057516990
Exac	rs1057516990
Gnomad	rs1057516990
Varsome	rs1057516990
LitVar	rs1057516990
Map	rs1057516990
PheGenI	rs1057516990
Biobank	rs1057516990
1000 genomes	rs1057516990
hgdp	rs1057516990
ensembl	rs1057516990
geneview	rs1057516990
scholar	rs1057516990
google	rs1057516990
pharmgkb	rs1057516990
gwascentral	rs1057516990
openSNP	rs1057516990
23andMe	rs1057516990
SNPshot	rs1057516990
SNPdbe	rs1057516990
MSV3d	rs1057516990
GWAS Ctlg	rs1057516990

Max Magnitude

0

ClinVar
Risk	rs1057516990(-;-)
Alt	rs1057516990(-;-)
Reference	Rs1057516990(T;T)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37429750delT
CLNSRC
CLNACC	RCV000409258.1,