rs180177319

Orientation

plus

Stabilized

plus

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

Make rs180177319(A;G)

Make rs180177319(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37424843

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177319
dbSNP (classic)	rs180177319
ClinGen	rs180177319
ebi	rs180177319
HLI	rs180177319
Exac	rs180177319
Gnomad	rs180177319
Varsome	rs180177319
LitVar	rs180177319
Map	rs180177319
PheGenI	rs180177319
Biobank	rs180177319
1000 genomes	rs180177319
hgdp	rs180177319
ensembl	rs180177319
geneview	rs180177319
scholar	rs180177319
google	rs180177319
pharmgkb	rs180177319
gwascentral	rs180177319
openSNP	rs180177319
23andMe	rs180177319
SNPshot	rs180177319
SNPdbe	rs180177319
MSV3d	rs180177319
GWAS Ctlg	rs180177319

Max Magnitude

0

ClinVar
Risk	rs180177319(G;G)
Alt	rs180177319(G;G)
Reference	Rs180177319(A;A)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37424840A>G
CLNSRC
CLNACC	RCV000186448.1,