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rs180177240

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177240(-;-)
Make rs180177240(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240873024
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177240
ebirs180177240
HLIrs180177240
Exacrs180177240
Varsomers180177240
Maprs180177240
PheGenIrs180177240
hapmaprs180177240
1000 genomesrs180177240
hgdprs180177240
ensemblrs180177240
gopubmedrs180177240
geneviewrs180177240
scholarrs180177240
googlers180177240
pharmgkbrs180177240
gwascentralrs180177240
openSNPrs180177240
23andMers180177240
23andMe allrs180177240
SNP Nexus

SNPshotrs180177240
SNPdbers180177240
MSV3drs180177240
GWAS Ctlgrs180177240
Max Magnitude0
ClinVar
Risk rs180177240(;)
Alt rs180177240(;)
Reference rs180177240(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812441delG
CLNSRC
CLNACC RCV000186397.1,