rs180177321

Orientation

plus

Stabilized

plus

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

Make rs180177321(-;-)

Make rs180177321(-;TG)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37432137

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177321
dbSNP (classic)	rs180177321
ClinGen	rs180177321
ebi	rs180177321
HLI	rs180177321
Exac	rs180177321
Gnomad	rs180177321
Varsome	rs180177321
LitVar	rs180177321
Map	rs180177321
PheGenI	rs180177321
Biobank	rs180177321
1000 genomes	rs180177321
hgdp	rs180177321
ensembl	rs180177321
geneview	rs180177321
scholar	rs180177321
google	rs180177321
pharmgkb	rs180177321
gwascentral	rs180177321
openSNP	rs180177321
23andMe	rs180177321
SNPshot	rs180177321
SNPdbe	rs180177321
MSV3d	rs180177321
GWAS Ctlg	rs180177321

Max Magnitude

0

ClinVar
Risk	rs180177321(-;-)
Alt	rs180177321(-;-)
Reference	Rs180177321(TG;TG)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37432134_37432135delTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149441.7,