rs180177322

Orientation

plus

Stabilized

plus

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

Make rs180177322(C;T)

Make rs180177322(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37436699

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177322
dbSNP (classic)	rs180177322
ClinGen	rs180177322
ebi	rs180177322
HLI	rs180177322
Exac	rs180177322
Gnomad	rs180177322
Varsome	rs180177322
LitVar	rs180177322
Map	rs180177322
PheGenI	rs180177322
Biobank	rs180177322
1000 genomes	rs180177322
hgdp	rs180177322
ensembl	rs180177322
geneview	rs180177322
scholar	rs180177322
google	rs180177322
pharmgkb	rs180177322
gwascentral	rs180177322
openSNP	rs180177322
23andMe	rs180177322
SNPshot	rs180177322
SNPdbe	rs180177322
MSV3d	rs180177322
GWAS Ctlg	rs180177322

Max Magnitude

0

ClinVar
Risk	rs180177322(T;T)
Alt	rs180177322(T;T)
Reference	Rs180177322(C;C)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37436696C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149443.5,