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rs180177158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177158(A;A)
Make rs180177158(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878151
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177158
ebirs180177158
HLIrs180177158
Exacrs180177158
Varsomers180177158
Maprs180177158
PheGenIrs180177158
hapmaprs180177158
1000 genomesrs180177158
hgdprs180177158
ensemblrs180177158
gopubmedrs180177158
geneviewrs180177158
scholarrs180177158
googlers180177158
pharmgkbrs180177158
gwascentralrs180177158
openSNPrs180177158
23andMers180177158
23andMe allrs180177158
SNP Nexus

SNPshotrs180177158
SNPdbers180177158
MSV3drs180177158
GWAS Ctlgrs180177158
Max Magnitude0
ClinVar
Risk rs180177158(A;A)
Alt rs180177158(A;A)
Reference rs180177158(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817568G>A
CLNSRC
CLNACC RCV000186369.1,