rs1057517238

Orientation

plus

Stabilized

plus

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

Make rs1057517238(-;A)

Make rs1057517238(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

37425935

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs1057517238
dbSNP (classic)	rs1057517238
ClinGen	rs1057517238
ebi	rs1057517238
HLI	rs1057517238
Exac	rs1057517238
Gnomad	rs1057517238
Varsome	rs1057517238
LitVar	rs1057517238
Map	rs1057517238
PheGenI	rs1057517238
Biobank	rs1057517238
1000 genomes	rs1057517238
hgdp	rs1057517238
ensembl	rs1057517238
geneview	rs1057517238
scholar	rs1057517238
google	rs1057517238
pharmgkb	rs1057517238
gwascentral	rs1057517238
openSNP	rs1057517238
23andMe	rs1057517238
SNPshot	rs1057517238
SNPdbe	rs1057517238
MSV3d	rs1057517238
GWAS Ctlg	rs1057517238

Max Magnitude

0

ClinVar
Risk	rs1057517238(A;A)
Alt	rs1057517238(A;A)
Reference	Rs1057517238(-;-)
Significance	Probable-Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37425932dupA
CLNSRC
CLNACC	RCV000411412.1,