rs1057517026

Orientation

plus

Stabilized

plus

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

Make rs1057517026(-;-)

Make rs1057517026(-;TG)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37428520

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057517026
dbSNP (classic)	rs1057517026
ClinGen	rs1057517026
ebi	rs1057517026
HLI	rs1057517026
Exac	rs1057517026
Gnomad	rs1057517026
Varsome	rs1057517026
LitVar	rs1057517026
Map	rs1057517026
PheGenI	rs1057517026
Biobank	rs1057517026
1000 genomes	rs1057517026
hgdp	rs1057517026
ensembl	rs1057517026
geneview	rs1057517026
scholar	rs1057517026
google	rs1057517026
pharmgkb	rs1057517026
gwascentral	rs1057517026
openSNP	rs1057517026
23andMe	rs1057517026
SNPshot	rs1057517026
SNPdbe	rs1057517026
MSV3d	rs1057517026
GWAS Ctlg	rs1057517026

Max Magnitude

0

ClinVar
Risk	rs1057517026(-;-)
Alt	rs1057517026(-;-)
Reference	Rs1057517026(TG;TG)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37428517_37428518delTG
CLNSRC
CLNACC	RCV000411789.1,