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rs180177297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177297(G;T)
Make rs180177297(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240877633
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177297
ebirs180177297
HLIrs180177297
Exacrs180177297
Varsomers180177297
Maprs180177297
PheGenIrs180177297
hapmaprs180177297
1000 genomesrs180177297
hgdprs180177297
ensemblrs180177297
gopubmedrs180177297
geneviewrs180177297
scholarrs180177297
googlers180177297
pharmgkbrs180177297
gwascentralrs180177297
openSNPrs180177297
23andMers180177297
23andMe allrs180177297
SNP Nexus

SNPshotrs180177297
SNPdbers180177297
MSV3drs180177297
GWAS Ctlgrs180177297
Max Magnitude0
ClinVar
Risk rs180177297(T;T)
Alt rs180177297(T;T)
Reference rs180177297(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817050G>T
CLNSRC
CLNACC RCV000186368.1,