rs180177294

Orientation

plus

Stabilized

plus

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

Make rs180177294(C;T)

Make rs180177294(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240877597

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177294
dbSNP (classic)	rs180177294
ClinGen	rs180177294
ebi	rs180177294
HLI	rs180177294
Exac	rs180177294
Gnomad	rs180177294
Varsome	rs180177294
LitVar	rs180177294
Map	rs180177294
PheGenI	rs180177294
Biobank	rs180177294
1000 genomes	rs180177294
hgdp	rs180177294
ensembl	rs180177294
geneview	rs180177294
scholar	rs180177294
google	rs180177294
pharmgkb	rs180177294
gwascentral	rs180177294
openSNP	rs180177294
23andMe	rs180177294
SNPshot	rs180177294
SNPdbe	rs180177294
MSV3d	rs180177294
GWAS Ctlg	rs180177294

Max Magnitude

0

ClinVar
Risk	rs180177294(T;T)
Alt	rs180177294(T;T)
Reference	Rs180177294(C;C)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241817014C>T
CLNSRC
CLNACC	RCV000186344.1,