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rs180177211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177211(A;G)
Make rs180177211(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240870656
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177211
ebirs180177211
HLIrs180177211
Exacrs180177211
Varsomers180177211
Maprs180177211
PheGenIrs180177211
hapmaprs180177211
1000 genomesrs180177211
hgdprs180177211
ensemblrs180177211
gopubmedrs180177211
geneviewrs180177211
scholarrs180177211
googlers180177211
pharmgkbrs180177211
gwascentralrs180177211
openSNPrs180177211
23andMers180177211
23andMe allrs180177211
SNP Nexus

SNPshotrs180177211
SNPdbers180177211
MSV3drs180177211
GWAS Ctlgrs180177211
Max Magnitude0
ClinVar
Risk rs180177211(C,G;C,G)
Alt rs180177211(C,G;C,G)
Reference rs180177211(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241810073A>C
CLNSRC
CLNACC RCV000186304.1,