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rs180177198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177198(A;A)
Make rs180177198(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869327
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177198
ebirs180177198
HLIrs180177198
Exacrs180177198
Varsomers180177198
Maprs180177198
PheGenIrs180177198
hapmaprs180177198
1000 genomesrs180177198
hgdprs180177198
ensemblrs180177198
gopubmedrs180177198
geneviewrs180177198
scholarrs180177198
googlers180177198
pharmgkbrs180177198
gwascentralrs180177198
openSNPrs180177198
23andMers180177198
23andMe allrs180177198
SNP Nexus

SNPshotrs180177198
SNPdbers180177198
MSV3drs180177198
GWAS Ctlgrs180177198
Max Magnitude0
ClinVar
Risk rs180177198(A;A)
Alt rs180177198(A;A)
Reference rs180177198(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808744G>A
CLNSRC
CLNACC RCV000186294.1,