rs180177168

Orientation

plus

Stabilized

plus

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

Make rs180177168(A;A)

Make rs180177168(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868987

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177168
dbSNP (classic)	rs180177168
ClinGen	rs180177168
ebi	rs180177168
HLI	rs180177168
Exac	rs180177168
Gnomad	rs180177168
Varsome	rs180177168
LitVar	rs180177168
Map	rs180177168
PheGenI	rs180177168
Biobank	rs180177168
1000 genomes	rs180177168
hgdp	rs180177168
ensembl	rs180177168
geneview	rs180177168
scholar	rs180177168
google	rs180177168
pharmgkb	rs180177168
gwascentral	rs180177168
openSNP	rs180177168
23andMe	rs180177168
SNPshot	rs180177168
SNPdbe	rs180177168
MSV3d	rs180177168
GWAS Ctlg	rs180177168

Merged from

Rs180177169

Max Magnitude

0

ClinVar
Risk	rs180177168(A;A) rs180177168(T;T)
Alt	rs180177168(A;A) rs180177168(T;T)
Reference	Rs180177168(G;G)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808404G>A; NC_000002.11:g.241808404G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000186279.1, RCV000169364.2,