rs180177304

Orientation

plus

Stabilized

plus

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

Make rs180177304(A;A)

Make rs180177304(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37424863

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177304
dbSNP (classic)	rs180177304
ClinGen	rs180177304
ebi	rs180177304
HLI	rs180177304
Exac	rs180177304
Gnomad	rs180177304
Varsome	rs180177304
LitVar	rs180177304
Map	rs180177304
PheGenI	rs180177304
Biobank	rs180177304
1000 genomes	rs180177304
hgdp	rs180177304
ensembl	rs180177304
geneview	rs180177304
scholar	rs180177304
google	rs180177304
pharmgkb	rs180177304
gwascentral	rs180177304
openSNP	rs180177304
23andMe	rs180177304
SNPshot	rs180177304
SNPdbe	rs180177304
MSV3d	rs180177304
GWAS Ctlg	rs180177304

Max Magnitude

0

ClinVar
Risk	rs180177304(A;A)
Alt	rs180177304(A;A)
Reference	Rs180177304(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37424860G>A
CLNSRC
CLNACC	RCV000186438.1,