rs180177236

Orientation

plus

Stabilized

plus

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

Make rs180177236(A;A)

Make rs180177236(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240873001

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177236
dbSNP (classic)	rs180177236
ClinGen	rs180177236
ebi	rs180177236
HLI	rs180177236
Exac	rs180177236
Gnomad	rs180177236
Varsome	rs180177236
LitVar	rs180177236
Map	rs180177236
PheGenI	rs180177236
Biobank	rs180177236
1000 genomes	rs180177236
hgdp	rs180177236
ensembl	rs180177236
geneview	rs180177236
scholar	rs180177236
google	rs180177236
pharmgkb	rs180177236
gwascentral	rs180177236
openSNP	rs180177236
23andMe	rs180177236
SNPshot	rs180177236
SNPdbe	rs180177236
MSV3d	rs180177236
GWAS Ctlg	rs180177236

Max Magnitude

0

ClinVar
Risk	rs180177236(A;A)
Alt	rs180177236(A;A)
Reference	Rs180177236(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241812418G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186317.1,