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rs180177185

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177185(C;C)
Make rs180177185(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869248
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177185
ebirs180177185
HLIrs180177185
Exacrs180177185
Varsomers180177185
Maprs180177185
PheGenIrs180177185
hapmaprs180177185
1000 genomesrs180177185
hgdprs180177185
ensemblrs180177185
gopubmedrs180177185
geneviewrs180177185
scholarrs180177185
googlers180177185
pharmgkbrs180177185
gwascentralrs180177185
openSNPrs180177185
23andMers180177185
23andMe allrs180177185
SNP Nexus

SNPshotrs180177185
SNPdbers180177185
MSV3drs180177185
GWAS Ctlgrs180177185
Max Magnitude0
ClinVar
Risk rs180177185(C;C)
Alt rs180177185(C;C)
Reference rs180177185(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808665G>C
CLNSRC
CLNACC RCV000186290.1,