rs180177308

Orientation

plus

Stabilized

plus

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

Make rs180177308(-;-)

Make rs180177308(-;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37426625

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177308
dbSNP (classic)	rs180177308
ClinGen	rs180177308
ebi	rs180177308
HLI	rs180177308
Exac	rs180177308
Gnomad	rs180177308
Varsome	rs180177308
LitVar	rs180177308
Map	rs180177308
PheGenI	rs180177308
Biobank	rs180177308
1000 genomes	rs180177308
hgdp	rs180177308
ensembl	rs180177308
geneview	rs180177308
scholar	rs180177308
google	rs180177308
pharmgkb	rs180177308
gwascentral	rs180177308
openSNP	rs180177308
23andMe	rs180177308
SNPshot	rs180177308
SNPdbe	rs180177308
MSV3d	rs180177308
GWAS Ctlg	rs180177308

Max Magnitude

0

ClinVar
Risk	rs180177308(-;-)
Alt	rs180177308(-;-)
Reference	Rs180177308(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37426622delG
CLNSRC
CLNACC	RCV000186456.1,