rs180177235

Orientation

plus

Stabilized

plus

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

Make rs180177235(A;A)

Make rs180177235(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240872987

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177235
dbSNP (classic)	rs180177235
ClinGen	rs180177235
ebi	rs180177235
HLI	rs180177235
Exac	rs180177235
Gnomad	rs180177235
Varsome	rs180177235
LitVar	rs180177235
Map	rs180177235
PheGenI	rs180177235
Biobank	rs180177235
1000 genomes	rs180177235
hgdp	rs180177235
ensembl	rs180177235
geneview	rs180177235
scholar	rs180177235
google	rs180177235
pharmgkb	rs180177235
gwascentral	rs180177235
openSNP	rs180177235
23andMe	rs180177235
SNPshot	rs180177235
SNPdbe	rs180177235
MSV3d	rs180177235
GWAS Ctlg	rs180177235

Max Magnitude

0

ClinVar
Risk	rs180177235(A;A)
Alt	rs180177235(A;A)
Reference	Rs180177235(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241812404G>A
CLNSRC
CLNACC	RCV000186316.1,