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rs180177236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177236(A;A)
Make rs180177236(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873001
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177236
ebirs180177236
HLIrs180177236
Exacrs180177236
Varsomers180177236
Maprs180177236
PheGenIrs180177236
hapmaprs180177236
1000 genomesrs180177236
hgdprs180177236
ensemblrs180177236
gopubmedrs180177236
geneviewrs180177236
scholarrs180177236
googlers180177236
pharmgkbrs180177236
gwascentralrs180177236
openSNPrs180177236
23andMers180177236
23andMe allrs180177236
SNP Nexus

SNPshotrs180177236
SNPdbers180177236
MSV3drs180177236
GWAS Ctlgrs180177236
Max Magnitude0
ClinVar
Risk rs180177236(A;A)
Alt rs180177236(A;A)
Reference rs180177236(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812418G>A
CLNSRC
CLNACC RCV000186317.1,