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rs180177157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177157(C;T)
Make rs180177157(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868971
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177157
ebirs180177157
HLIrs180177157
Exacrs180177157
Varsomers180177157
Maprs180177157
PheGenIrs180177157
hapmaprs180177157
1000 genomesrs180177157
hgdprs180177157
ensemblrs180177157
gopubmedrs180177157
geneviewrs180177157
scholarrs180177157
googlers180177157
pharmgkbrs180177157
gwascentralrs180177157
openSNPrs180177157
23andMers180177157
23andMe allrs180177157
SNP Nexus

SNPshotrs180177157
SNPdbers180177157
MSV3drs180177157
GWAS Ctlgrs180177157
Max Magnitude0
ClinVar
Risk rs180177157(T;T)
Alt rs180177157(T;T)
Reference rs180177157(C;C)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808388C>T
CLNSRC
CLNACC RCV000169332.2,