rs180177157

Orientation

plus

Stabilized

plus

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

Make rs180177157(C;T)

Make rs180177157(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868971

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177157
dbSNP (classic)	rs180177157
ClinGen	rs180177157
ebi	rs180177157
HLI	rs180177157
Exac	rs180177157
Gnomad	rs180177157
Varsome	rs180177157
LitVar	rs180177157
Map	rs180177157
PheGenI	rs180177157
Biobank	rs180177157
1000 genomes	rs180177157
hgdp	rs180177157
ensembl	rs180177157
geneview	rs180177157
scholar	rs180177157
google	rs180177157
pharmgkb	rs180177157
gwascentral	rs180177157
openSNP	rs180177157
23andMe	rs180177157
SNPshot	rs180177157
SNPdbe	rs180177157
MSV3d	rs180177157
GWAS Ctlg	rs180177157

Max Magnitude

0

ClinVar
Risk	rs180177157(T;T)
Alt	rs180177157(T;T)
Reference	Rs180177157(C;C)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808388C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000169332.2,