rs180177156

Orientation

plus

Stabilized

plus

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

Make rs180177156(A;A)

Make rs180177156(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878128

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177156
dbSNP (classic)	rs180177156
ClinGen	rs180177156
ebi	rs180177156
HLI	rs180177156
Exac	rs180177156
Gnomad	rs180177156
Varsome	rs180177156
LitVar	rs180177156
Map	rs180177156
PheGenI	rs180177156
Biobank	rs180177156
1000 genomes	rs180177156
hgdp	rs180177156
ensembl	rs180177156
geneview	rs180177156
scholar	rs180177156
google	rs180177156
pharmgkb	rs180177156
gwascentral	rs180177156
openSNP	rs180177156
23andMe	rs180177156
SNPshot	rs180177156
SNPdbe	rs180177156
MSV3d	rs180177156
GWAS Ctlg	rs180177156

Max Magnitude

0

ClinVar
Risk	rs180177156(A;A) rs180177156(T;T)
Alt	rs180177156(A;A) rs180177156(T;T)
Reference	Rs180177156(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817545G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169365.2,