rs180177190

Orientation

plus

Stabilized

plus

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

Make rs180177190(-;GAG)

Make rs180177190(GAG;GAG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240869289

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177190
dbSNP (classic)	rs180177190
ClinGen	rs180177190
ebi	rs180177190
HLI	rs180177190
Exac	rs180177190
Gnomad	rs180177190
Varsome	rs180177190
LitVar	rs180177190
Map	rs180177190
PheGenI	rs180177190
Biobank	rs180177190
1000 genomes	rs180177190
hgdp	rs180177190
ensembl	rs180177190
geneview	rs180177190
scholar	rs180177190
google	rs180177190
pharmgkb	rs180177190
gwascentral	rs180177190
openSNP	rs180177190
23andMe	rs180177190
SNPshot	rs180177190
SNPdbe	rs180177190
MSV3d	rs180177190
GWAS Ctlg	rs180177190

Max Magnitude

0

ClinVar
Risk	rs180177190(GGA;GGA)
Alt	rs180177190(GGA;GGA)
Reference	Rs180177190(-;-)
Significance	Pathogenic
Disease	Primary hyperoxaluria
Variation	info
Gene	AGXT
CLNDBN	Primary hyperoxaluria, type I
Reversed	0
HGVS	NC_000002.11:g.241808704_241808706dupGAG
CLNSRC
CLNACC	RCV000186387.1,