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rs180177202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177202(C;T)
Make rs180177202(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869335
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177202
ebirs180177202
HLIrs180177202
Exacrs180177202
Varsomers180177202
Maprs180177202
PheGenIrs180177202
hapmaprs180177202
1000 genomesrs180177202
hgdprs180177202
ensemblrs180177202
gopubmedrs180177202
geneviewrs180177202
scholarrs180177202
googlers180177202
pharmgkbrs180177202
gwascentralrs180177202
openSNPrs180177202
23andMers180177202
23andMe allrs180177202
SNP Nexus

SNPshotrs180177202
SNPdbers180177202
MSV3drs180177202
GWAS Ctlgrs180177202
Max Magnitude0
ClinVar
Risk rs180177202(A,T;A,T)
Alt rs180177202(A,T;A,T)
Reference rs180177202(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808752C>T
CLNSRC
CLNACC RCV000186297.1,