rs1057516823

Orientation

plus

Stabilized

plus

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

Make rs1057516823(-;A)

Make rs1057516823(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37432028

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057516823
dbSNP (classic)	rs1057516823
ClinGen	rs1057516823
ebi	rs1057516823
HLI	rs1057516823
Exac	rs1057516823
Gnomad	rs1057516823
Varsome	rs1057516823
LitVar	rs1057516823
Map	rs1057516823
PheGenI	rs1057516823
Biobank	rs1057516823
1000 genomes	rs1057516823
hgdp	rs1057516823
ensembl	rs1057516823
geneview	rs1057516823
scholar	rs1057516823
google	rs1057516823
pharmgkb	rs1057516823
gwascentral	rs1057516823
openSNP	rs1057516823
23andMe	rs1057516823
SNPshot	rs1057516823
SNPdbe	rs1057516823
MSV3d	rs1057516823
GWAS Ctlg	rs1057516823

Max Magnitude

0

ClinVar
Risk	rs1057516823(A;A)
Alt	rs1057516823(A;A)
Reference	Rs1057516823(-;-)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37432025dupA
CLNSRC
CLNACC	RCV000409413.1,