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rs180177269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177269(A;A)
Make rs180177269(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875941
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177269
ebirs180177269
HLIrs180177269
Exacrs180177269
Varsomers180177269
Maprs180177269
PheGenIrs180177269
hapmaprs180177269
1000 genomesrs180177269
hgdprs180177269
ensemblrs180177269
gopubmedrs180177269
geneviewrs180177269
scholarrs180177269
googlers180177269
pharmgkbrs180177269
gwascentralrs180177269
openSNPrs180177269
23andMers180177269
23andMe allrs180177269
SNP Nexus

SNPshotrs180177269
SNPdbers180177269
MSV3drs180177269
GWAS Ctlgrs180177269
Max Magnitude0
ClinVar
Risk rs180177269(A;A)
Alt rs180177269(A;A)
Reference rs180177269(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815358T>A
CLNSRC
CLNACC RCV000186333.1,