rs180177316

Orientation

plus

Stabilized

plus

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

Make rs180177316(-;-)

Make rs180177316(-;CT)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37430520

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177316
dbSNP (classic)	rs180177316
ClinGen	rs180177316
ebi	rs180177316
HLI	rs180177316
Exac	rs180177316
Gnomad	rs180177316
Varsome	rs180177316
LitVar	rs180177316
Map	rs180177316
PheGenI	rs180177316
Biobank	rs180177316
1000 genomes	rs180177316
hgdp	rs180177316
ensembl	rs180177316
geneview	rs180177316
scholar	rs180177316
google	rs180177316
pharmgkb	rs180177316
gwascentral	rs180177316
openSNP	rs180177316
23andMe	rs180177316
SNPshot	rs180177316
SNPdbe	rs180177316
MSV3d	rs180177316
GWAS Ctlg	rs180177316

Max Magnitude

0

ClinVar
Risk	rs180177316(-;-)
Alt	rs180177316(-;-)
Reference	Rs180177316(CT;CT)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37430517_37430518delCT
CLNSRC
CLNACC	RCV000186459.1,