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rs180177239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177239(A;A)
Make rs180177239(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873022
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177239
ebirs180177239
HLIrs180177239
Exacrs180177239
Varsomers180177239
Maprs180177239
PheGenIrs180177239
hapmaprs180177239
1000 genomesrs180177239
hgdprs180177239
ensemblrs180177239
gopubmedrs180177239
geneviewrs180177239
scholarrs180177239
googlers180177239
pharmgkbrs180177239
gwascentralrs180177239
openSNPrs180177239
23andMers180177239
23andMe allrs180177239
SNP Nexus

SNPshotrs180177239
SNPdbers180177239
MSV3drs180177239
GWAS Ctlgrs180177239
Max Magnitude0
ClinVar
Risk rs180177239(A;A)
Alt rs180177239(A;A)
Reference rs180177239(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812439G>A
CLNSRC
CLNACC RCV000169439.2,