rs180177203

Orientation

plus

Stabilized

plus

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

Make rs180177203(A;A)

Make rs180177203(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

240869336

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177203
dbSNP (classic)	rs180177203
ClinGen	rs180177203
ebi	rs180177203
HLI	rs180177203
Exac	rs180177203
Gnomad	rs180177203
Varsome	rs180177203
LitVar	rs180177203
Map	rs180177203
PheGenI	rs180177203
Biobank	rs180177203
1000 genomes	rs180177203
hgdp	rs180177203
ensembl	rs180177203
geneview	rs180177203
scholar	rs180177203
google	rs180177203
pharmgkb	rs180177203
gwascentral	rs180177203
openSNP	rs180177203
23andMe	rs180177203
SNPshot	rs180177203
SNPdbe	rs180177203
MSV3d	rs180177203
GWAS Ctlg	rs180177203

Max Magnitude

0

ClinVar
Risk	rs180177203(A;A) rs180177203(T;T)
Alt	rs180177203(A;A) rs180177203(T;T)
Reference	Rs180177203(G;G)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808753G>A
CLNSRC
CLNACC	RCV000186298.1,