rs180177315

Orientation

plus

Stabilized

plus

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

Make rs180177315(-;-)

Make rs180177315(-;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

37429778

Gene

GRHPR

is a	snp
is	mentioned by
dbSNP	rs180177315
dbSNP (classic)	rs180177315
ClinGen	rs180177315
ebi	rs180177315
HLI	rs180177315
Exac	rs180177315
Gnomad	rs180177315
Varsome	rs180177315
LitVar	rs180177315
Map	rs180177315
PheGenI	rs180177315
Biobank	rs180177315
1000 genomes	rs180177315
hgdp	rs180177315
ensembl	rs180177315
geneview	rs180177315
scholar	rs180177315
google	rs180177315
pharmgkb	rs180177315
gwascentral	rs180177315
openSNP	rs180177315
23andMe	rs180177315
SNPshot	rs180177315
SNPdbe	rs180177315
MSV3d	rs180177315
GWAS Ctlg	rs180177315

Max Magnitude

0

ClinVar
Risk	rs180177315(-;-)
Alt	rs180177315(-;-)
Reference	Rs180177315(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	GRHPR
CLNDBN	Primary hyperoxaluria, type II
Reversed	0
HGVS	NC_000009.11:g.37429775delT
CLNSRC
CLNACC	RCV000186458.1,