rs180177317

Orientation

plus

Stabilized

plus

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

Make rs180177317(A;A)

Make rs180177317(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37432007

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177317
dbSNP (classic)	rs180177317
ClinGen	rs180177317
ebi	rs180177317
HLI	rs180177317
Exac	rs180177317
Gnomad	rs180177317
Varsome	rs180177317
LitVar	rs180177317
Map	rs180177317
PheGenI	rs180177317
Biobank	rs180177317
1000 genomes	rs180177317
hgdp	rs180177317
ensembl	rs180177317
geneview	rs180177317
scholar	rs180177317
google	rs180177317
pharmgkb	rs180177317
gwascentral	rs180177317
openSNP	rs180177317
23andMe	rs180177317
SNPshot	rs180177317
SNPdbe	rs180177317
MSV3d	rs180177317
GWAS Ctlg	rs180177317

Max Magnitude

0

ClinVar
Risk	rs180177317(A;A)
Alt	rs180177317(A;A)
Reference	Rs180177317(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37432004G>A
CLNSRC
CLNACC	RCV000186451.1,