rs180177225

Orientation

plus

Stabilized

plus

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

Make rs180177225(A;A)

Make rs180177225(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240871398

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177225
dbSNP (classic)	rs180177225
ClinGen	rs180177225
ebi	rs180177225
HLI	rs180177225
Exac	rs180177225
Gnomad	rs180177225
Varsome	rs180177225
LitVar	rs180177225
Map	rs180177225
PheGenI	rs180177225
Biobank	rs180177225
1000 genomes	rs180177225
hgdp	rs180177225
ensembl	rs180177225
geneview	rs180177225
scholar	rs180177225
google	rs180177225
pharmgkb	rs180177225
gwascentral	rs180177225
openSNP	rs180177225
23andMe	rs180177225
SNPshot	rs180177225
SNPdbe	rs180177225
MSV3d	rs180177225
GWAS Ctlg	rs180177225

Merged from

Rs180177226

Max Magnitude

0

ClinVar
Risk	rs180177225(A;A) rs180177225(T;T)
Alt	rs180177225(A;A) rs180177225(T;T)
Reference	Rs180177225(C;C)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241810815C>A; NC_000002.11:g.241810815C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186310.1, RCV000186309.1,