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rs180177258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177258(C;C)
Make rs180177258(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875155
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177258
ebirs180177258
HLIrs180177258
Exacrs180177258
Varsomers180177258
Maprs180177258
PheGenIrs180177258
hapmaprs180177258
1000 genomesrs180177258
hgdprs180177258
ensemblrs180177258
gopubmedrs180177258
geneviewrs180177258
scholarrs180177258
googlers180177258
pharmgkbrs180177258
gwascentralrs180177258
openSNPrs180177258
23andMers180177258
23andMe allrs180177258
SNP Nexus

SNPshotrs180177258
SNPdbers180177258
MSV3drs180177258
GWAS Ctlgrs180177258
Max Magnitude0
ClinVar
Risk rs180177258(C;C)
Alt rs180177258(C;C)
Reference rs180177258(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814572G>C
CLNSRC
CLNACC RCV000186330.1,