rs180177318

Orientation

plus

Stabilized

plus

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

Make rs180177318(A;G)

Make rs180177318(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37432013

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177318
dbSNP (classic)	rs180177318
ClinGen	rs180177318
ebi	rs180177318
HLI	rs180177318
Exac	rs180177318
Gnomad	rs180177318
Varsome	rs180177318
LitVar	rs180177318
Map	rs180177318
PheGenI	rs180177318
Biobank	rs180177318
1000 genomes	rs180177318
hgdp	rs180177318
ensembl	rs180177318
geneview	rs180177318
scholar	rs180177318
google	rs180177318
pharmgkb	rs180177318
gwascentral	rs180177318
openSNP	rs180177318
23andMe	rs180177318
SNPshot	rs180177318
SNPdbe	rs180177318
MSV3d	rs180177318
GWAS Ctlg	rs180177318

Max Magnitude

0

ClinVar
Risk	rs180177318(G;G)
Alt	rs180177318(G;G)
Reference	Rs180177318(A;A)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37432010A>G
CLNSRC
CLNACC	RCV000186433.1,