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rs180177261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177261(-;-)
Make rs180177261(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875172
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177261
ebirs180177261
HLIrs180177261
Exacrs180177261
Varsomers180177261
Maprs180177261
PheGenIrs180177261
hapmaprs180177261
1000 genomesrs180177261
hgdprs180177261
ensemblrs180177261
gopubmedrs180177261
geneviewrs180177261
scholarrs180177261
googlers180177261
pharmgkbrs180177261
gwascentralrs180177261
openSNPrs180177261
23andMers180177261
23andMe allrs180177261
SNP Nexus

SNPshotrs180177261
SNPdbers180177261
MSV3drs180177261
GWAS Ctlgrs180177261
Max Magnitude0
ClinVar
Risk rs180177261(;)
Alt rs180177261(;)
Reference rs180177261(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814589delC
CLNSRC
CLNACC RCV000186405.1,