rs1057516941

Orientation

plus

Stabilized

plus

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

Make rs1057516941(-;A)

Make rs1057516941(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37428533

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516941
dbSNP (classic)	rs1057516941
ClinGen	rs1057516941
ebi	rs1057516941
HLI	rs1057516941
Exac	rs1057516941
Gnomad	rs1057516941
Varsome	rs1057516941
LitVar	rs1057516941
Map	rs1057516941
PheGenI	rs1057516941
Biobank	rs1057516941
1000 genomes	rs1057516941
hgdp	rs1057516941
ensembl	rs1057516941
geneview	rs1057516941
scholar	rs1057516941
google	rs1057516941
pharmgkb	rs1057516941
gwascentral	rs1057516941
openSNP	rs1057516941
23andMe	rs1057516941
SNPshot	rs1057516941
SNPdbe	rs1057516941
MSV3d	rs1057516941
GWAS Ctlg	rs1057516941

Max Magnitude

0

ClinVar
Risk	rs1057516941(A;A)
Alt	rs1057516941(A;A)
Reference	Rs1057516941(-;-)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37428530dupA
CLNSRC
CLNACC	RCV000411634.1,