rs180177305

Orientation

plus

Stabilized

plus

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

Make rs180177305(C;C)

Make rs180177305(C;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37424964

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177305
dbSNP (classic)	rs180177305
ClinGen	rs180177305
ebi	rs180177305
HLI	rs180177305
Exac	rs180177305
Gnomad	rs180177305
Varsome	rs180177305
LitVar	rs180177305
Map	rs180177305
PheGenI	rs180177305
Biobank	rs180177305
1000 genomes	rs180177305
hgdp	rs180177305
ensembl	rs180177305
geneview	rs180177305
scholar	rs180177305
google	rs180177305
pharmgkb	rs180177305
gwascentral	rs180177305
openSNP	rs180177305
23andMe	rs180177305
SNPshot	rs180177305
SNPdbe	rs180177305
MSV3d	rs180177305
GWAS Ctlg	rs180177305

Max Magnitude

0

ClinVar
Risk	rs180177305(C;C)
Alt	rs180177305(C;C)
Reference	Rs180177305(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37424961T>C
CLNSRC
CLNACC	RCV000186439.1,