rs180177166

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(;)	0	common in clinvar
(-;-)	0	common/normal

Make rs180177166(-;CA)

Make rs180177166(CA;CA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240868982

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177166
dbSNP (classic)	rs180177166
ClinGen	rs180177166
ebi	rs180177166
HLI	rs180177166
Exac	rs180177166
Gnomad	rs180177166
Varsome	rs180177166
LitVar	rs180177166
Map	rs180177166
PheGenI	rs180177166
Biobank	rs180177166
1000 genomes	rs180177166
hgdp	rs180177166
ensembl	rs180177166
geneview	rs180177166
scholar	rs180177166
google	rs180177166
pharmgkb	rs180177166
gwascentral	rs180177166
openSNP	rs180177166
23andMe	rs180177166
SNPshot	rs180177166
SNPdbe	rs180177166
MSV3d	rs180177166
GWAS Ctlg	rs180177166

Max Magnitude

0

ClinVar
Risk	rs180177166(CA;CA)
Alt	rs180177166(CA;CA)
Reference	Rs180177166(-;-)
Significance	Other
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808398_241808399dupCA
CLNSRC
CLNACC	RCV000186382.1,