rs180177195

Orientation

plus

Stabilized

plus

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

Make rs180177195(C;C)

Make rs180177195(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869306

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177195
dbSNP (classic)	rs180177195
ClinGen	rs180177195
ebi	rs180177195
HLI	rs180177195
Exac	rs180177195
Gnomad	rs180177195
Varsome	rs180177195
LitVar	rs180177195
Map	rs180177195
PheGenI	rs180177195
Biobank	rs180177195
1000 genomes	rs180177195
hgdp	rs180177195
ensembl	rs180177195
geneview	rs180177195
scholar	rs180177195
google	rs180177195
pharmgkb	rs180177195
gwascentral	rs180177195
openSNP	rs180177195
23andMe	rs180177195
SNPshot	rs180177195
SNPdbe	rs180177195
MSV3d	rs180177195
GWAS Ctlg	rs180177195

Max Magnitude

0

ClinVar
Risk	rs180177195(C;C)
Alt	rs180177195(C;C)
Reference	Rs180177195(T;T)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808723T>C
CLNSRC
CLNACC	RCV000169219.2,