rs180177312

Orientation

plus

Stabilized

plus

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

Make rs180177312(A;A)

Make rs180177312(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37428557

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177312
dbSNP (classic)	rs180177312
ClinGen	rs180177312
ebi	rs180177312
HLI	rs180177312
Exac	rs180177312
Gnomad	rs180177312
Varsome	rs180177312
LitVar	rs180177312
Map	rs180177312
PheGenI	rs180177312
Biobank	rs180177312
1000 genomes	rs180177312
hgdp	rs180177312
ensembl	rs180177312
geneview	rs180177312
scholar	rs180177312
google	rs180177312
pharmgkb	rs180177312
gwascentral	rs180177312
openSNP	rs180177312
23andMe	rs180177312
SNPshot	rs180177312
SNPdbe	rs180177312
MSV3d	rs180177312
GWAS Ctlg	rs180177312

Max Magnitude

0

ClinVar
Risk	rs180177312(A;A)
Alt	rs180177312(A;A)
Reference	Rs180177312(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37428554G>A
CLNSRC
CLNACC	RCV000186441.1,