rs180177309

Orientation

plus

Stabilized

plus

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

Make rs180177309(-;-)

Make rs180177309(-;AAGT)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37426653

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177309
dbSNP (classic)	rs180177309
ClinGen	rs180177309
ebi	rs180177309
HLI	rs180177309
Exac	rs180177309
Gnomad	rs180177309
Varsome	rs180177309
LitVar	rs180177309
Map	rs180177309
PheGenI	rs180177309
Biobank	rs180177309
1000 genomes	rs180177309
hgdp	rs180177309
ensembl	rs180177309
geneview	rs180177309
scholar	rs180177309
google	rs180177309
pharmgkb	rs180177309
gwascentral	rs180177309
openSNP	rs180177309
23andMe	rs180177309
SNPshot	rs180177309
SNPdbe	rs180177309
MSV3d	rs180177309
GWAS Ctlg	rs180177309

Merged from

Rs180177310

Max Magnitude

0

ClinVar
Risk	rs180177309(-;-) rs180177309(GTAA;GTAA)
Alt	rs180177309(-;-) rs180177309(GTAA;GTAA)
Reference	Rs180177309(AAGT;AAGT)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37426654_37426657delAAGT
CLNSRC
CLNACC	RCV000186457.2,

[PMID 14635115] Molecular analysis of the glyoxylate reductase (GRHPR) gene and description of mutations underlying primary hyperoxaluria type 2.