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rs180177170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177170(A;A)
Make rs180177170(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868990
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177170
ebirs180177170
HLIrs180177170
Exacrs180177170
Varsomers180177170
Maprs180177170
PheGenIrs180177170
hapmaprs180177170
1000 genomesrs180177170
hgdprs180177170
ensemblrs180177170
gopubmedrs180177170
geneviewrs180177170
scholarrs180177170
googlers180177170
pharmgkbrs180177170
gwascentralrs180177170
openSNPrs180177170
23andMers180177170
23andMe allrs180177170
SNP Nexus

SNPshotrs180177170
SNPdbers180177170
MSV3drs180177170
GWAS Ctlgrs180177170
Max Magnitude0
ClinVar
Risk rs180177170(A;A)
Alt rs180177170(A;A)
Reference rs180177170(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808407G>A
CLNSRC
CLNACC RCV000186280.1,