rs180177207

Orientation

plus

Stabilized

plus

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

Make rs180177207(A;A)

Make rs180177207(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869350

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177207
dbSNP (classic)	rs180177207
ClinGen	rs180177207
ebi	rs180177207
HLI	rs180177207
Exac	rs180177207
Gnomad	rs180177207
Varsome	rs180177207
LitVar	rs180177207
Map	rs180177207
PheGenI	rs180177207
Biobank	rs180177207
1000 genomes	rs180177207
hgdp	rs180177207
ensembl	rs180177207
geneview	rs180177207
scholar	rs180177207
google	rs180177207
pharmgkb	rs180177207
gwascentral	rs180177207
openSNP	rs180177207
23andMe	rs180177207
SNPshot	rs180177207
SNPdbe	rs180177207
MSV3d	rs180177207
GWAS Ctlg	rs180177207

Max Magnitude

0

ClinVar
Risk	rs180177207(A;A)
Alt	rs180177207(A;A)
Reference	Rs180177207(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808767G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169408.2,