rs180177314

Orientation

plus

Stabilized

plus

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

Make rs180177314(A;A)

Make rs180177314(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37429732

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177314
dbSNP (classic)	rs180177314
ClinGen	rs180177314
ebi	rs180177314
HLI	rs180177314
Exac	rs180177314
Gnomad	rs180177314
Varsome	rs180177314
LitVar	rs180177314
Map	rs180177314
PheGenI	rs180177314
Biobank	rs180177314
1000 genomes	rs180177314
hgdp	rs180177314
ensembl	rs180177314
geneview	rs180177314
scholar	rs180177314
google	rs180177314
pharmgkb	rs180177314
gwascentral	rs180177314
openSNP	rs180177314
23andMe	rs180177314
SNPshot	rs180177314
SNPdbe	rs180177314
MSV3d	rs180177314
GWAS Ctlg	rs180177314

Max Magnitude

0

ClinVar
Risk	rs180177314(A;A)
Alt	rs180177314(A;A)
Reference	Rs180177314(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37429729G>A
CLNSRC
CLNACC	RCV000186442.1,