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rs180177186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177186(A;G)
Make rs180177186(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869252
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177186
ebirs180177186
HLIrs180177186
Exacrs180177186
Varsomers180177186
Maprs180177186
PheGenIrs180177186
hapmaprs180177186
1000 genomesrs180177186
hgdprs180177186
ensemblrs180177186
gopubmedrs180177186
geneviewrs180177186
scholarrs180177186
googlers180177186
pharmgkbrs180177186
gwascentralrs180177186
openSNPrs180177186
23andMers180177186
23andMe allrs180177186
SNP Nexus

SNPshotrs180177186
SNPdbers180177186
MSV3drs180177186
GWAS Ctlgrs180177186
Max Magnitude0
ClinVar
Risk rs180177186(G;G)
Alt rs180177186(G;G)
Reference rs180177186(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808669A>G
CLNSRC
CLNACC RCV000186291.1,