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rs180177235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177235(A;A)
Make rs180177235(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240872987
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177235
ebirs180177235
HLIrs180177235
Exacrs180177235
Varsomers180177235
Maprs180177235
PheGenIrs180177235
hapmaprs180177235
1000 genomesrs180177235
hgdprs180177235
ensemblrs180177235
gopubmedrs180177235
geneviewrs180177235
scholarrs180177235
googlers180177235
pharmgkbrs180177235
gwascentralrs180177235
openSNPrs180177235
23andMers180177235
23andMe allrs180177235
SNP Nexus

SNPshotrs180177235
SNPdbers180177235
MSV3drs180177235
GWAS Ctlgrs180177235
Max Magnitude0
ClinVar
Risk rs180177235(A;A)
Alt rs180177235(A;A)
Reference rs180177235(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812404G>A
CLNSRC
CLNACC RCV000186316.1,