rs180177229

Merged into

rs180177227

Orientation

plus

Stabilized

plus

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

Make rs180177229(G;T)

Make rs180177229(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

240871406

Gene

AGXT

is a	snp
is	mentioned by
dbSNP	rs180177229
dbSNP (classic)	rs180177229
ClinGen	rs180177229
ebi	rs180177229
HLI	rs180177229
Exac	rs180177229
Gnomad	rs180177229
Varsome	rs180177229
LitVar	rs180177229
Map	rs180177229
PheGenI	rs180177229
Biobank	rs180177229
1000 genomes	rs180177229
hgdp	rs180177229
ensembl	rs180177229
geneview	rs180177229
scholar	rs180177229
google	rs180177229
pharmgkb	rs180177229
gwascentral	rs180177229
openSNP	rs180177229
23andMe	rs180177229
SNPshot	rs180177229
SNPdbe	rs180177229
MSV3d	rs180177229
GWAS Ctlg	rs180177229

Status

Merged into rs180177227

Max Magnitude

0

ClinVar
Risk	rs180177229(T;T)
Alt	rs180177229(T;T)
Reference	Rs180177229(G;G)
Significance	Pathogenic
Disease
Variation	info
Gene	AGXT
CLNDBN	OMIM
Reversed	0
HGVS	NC_000002.11:g.241810823G>T
CLNSRC
CLNACC