rs180177165

Orientation

plus

Stabilized

plus

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

Make rs180177165(C;C)

Make rs180177165(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240878793

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177165
dbSNP (classic)	rs180177165
ClinGen	rs180177165
ebi	rs180177165
HLI	rs180177165
Exac	rs180177165
Gnomad	rs180177165
Varsome	rs180177165
LitVar	rs180177165
Map	rs180177165
PheGenI	rs180177165
Biobank	rs180177165
1000 genomes	rs180177165
hgdp	rs180177165
ensembl	rs180177165
geneview	rs180177165
scholar	rs180177165
google	rs180177165
pharmgkb	rs180177165
gwascentral	rs180177165
openSNP	rs180177165
23andMe	rs180177165
SNPshot	rs180177165
SNPdbe	rs180177165
MSV3d	rs180177165
GWAS Ctlg	rs180177165

Max Magnitude

0

ClinVar
Risk	rs180177165(C;C)
Alt	rs180177165(C;C)
Reference	Rs180177165(T;T)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241818210T>C
CLNSRC
CLNACC	RCV000186357.1,