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rs180177200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177200(-;-)
Make rs180177200(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869331
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177200
ebirs180177200
HLIrs180177200
Exacrs180177200
Varsomers180177200
Maprs180177200
PheGenIrs180177200
hapmaprs180177200
1000 genomesrs180177200
hgdprs180177200
ensemblrs180177200
gopubmedrs180177200
geneviewrs180177200
scholarrs180177200
googlers180177200
pharmgkbrs180177200
gwascentralrs180177200
openSNPrs180177200
23andMers180177200
23andMe allrs180177200
SNP Nexus

SNPshotrs180177200
SNPdbers180177200
MSV3drs180177200
GWAS Ctlgrs180177200
Max Magnitude0
ClinVar
Risk rs180177200(;)
Alt rs180177200(;)
Reference rs180177200(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808748delG
CLNSRC
CLNACC RCV000186389.1,