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rs180177196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177196(A;A)
Make rs180177196(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869312
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177196
ebirs180177196
HLIrs180177196
Exacrs180177196
Varsomers180177196
Maprs180177196
PheGenIrs180177196
hapmaprs180177196
1000 genomesrs180177196
hgdprs180177196
ensemblrs180177196
gopubmedrs180177196
geneviewrs180177196
scholarrs180177196
googlers180177196
pharmgkbrs180177196
gwascentralrs180177196
openSNPrs180177196
23andMers180177196
23andMe allrs180177196
SNP Nexus

SNPshotrs180177196
SNPdbers180177196
MSV3drs180177196
GWAS Ctlgrs180177196
Max Magnitude0
ClinVar
Risk rs180177196(A;A)
Alt rs180177196(A;A)
Reference rs180177196(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808729G>A
CLNSRC
CLNACC RCV000186388.1,