rs180177323

Orientation

plus

Stabilized

plus

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

Make rs180177323(A;A)

Make rs180177323(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37436700

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177323
dbSNP (classic)	rs180177323
ClinGen	rs180177323
ebi	rs180177323
HLI	rs180177323
Exac	rs180177323
Gnomad	rs180177323
Varsome	rs180177323
LitVar	rs180177323
Map	rs180177323
PheGenI	rs180177323
Biobank	rs180177323
1000 genomes	rs180177323
hgdp	rs180177323
ensembl	rs180177323
geneview	rs180177323
scholar	rs180177323
google	rs180177323
pharmgkb	rs180177323
gwascentral	rs180177323
openSNP	rs180177323
23andMe	rs180177323
SNPshot	rs180177323
SNPdbe	rs180177323
MSV3d	rs180177323
GWAS Ctlg	rs180177323

Max Magnitude

0

ClinVar
Risk	rs180177323(A;A)
Alt	rs180177323(A;A)
Reference	Rs180177323(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37436697G>A
CLNSRC
CLNACC	RCV000186444.1,