rs180177325

Orientation

plus

Stabilized

plus

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

Make rs180177325(C;C)

Make rs180177325(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

37436760

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177325
dbSNP (classic)	rs180177325
ClinGen	rs180177325
ebi	rs180177325
HLI	rs180177325
Exac	rs180177325
Gnomad	rs180177325
Varsome	rs180177325
LitVar	rs180177325
Map	rs180177325
PheGenI	rs180177325
Biobank	rs180177325
1000 genomes	rs180177325
hgdp	rs180177325
ensembl	rs180177325
geneview	rs180177325
scholar	rs180177325
google	rs180177325
pharmgkb	rs180177325
gwascentral	rs180177325
openSNP	rs180177325
23andMe	rs180177325
SNPshot	rs180177325
SNPdbe	rs180177325
MSV3d	rs180177325
GWAS Ctlg	rs180177325

Max Magnitude

0

ClinVar
Risk	rs180177325(C;C) rs180177325(G;G)
Alt	rs180177325(C;C) rs180177325(G;G)
Reference	Rs180177325(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37436757T>C; NC_000009.11:g.37436757T>G
CLNSRC
CLNACC	RCV000186447.1, RCV000186446.1,