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rs180177201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs180177201(-;-)
Make rs180177201(-;CC)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868897
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177201
ebirs180177201
HLIrs180177201
Exacrs180177201
Varsomers180177201
Maprs180177201
PheGenIrs180177201
hapmaprs180177201
1000 genomesrs180177201
hgdprs180177201
ensemblrs180177201
gopubmedrs180177201
geneviewrs180177201
scholarrs180177201
googlers180177201
pharmgkbrs180177201
gwascentralrs180177201
openSNPrs180177201
23andMers180177201
23andMe allrs180177201
SNP Nexus

SNPshotrs180177201
SNPdbers180177201
MSV3drs180177201
GWAS Ctlgrs180177201
Max Magnitude0
ClinVar
Risk rs180177201(;)
Alt rs180177201(;)
Reference rs180177201(CC;CC)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808314_241808315delCC
CLNSRC
CLNACC RCV000186380.1,