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rs180177257

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs180177257(-;-)
Make rs180177257(-;T)
Make rs180177257(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875153
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177257
ebirs180177257
HLIrs180177257
Exacrs180177257
Varsomers180177257
Maprs180177257
PheGenIrs180177257
hapmaprs180177257
1000 genomesrs180177257
hgdprs180177257
ensemblrs180177257
gopubmedrs180177257
geneviewrs180177257
scholarrs180177257
googlers180177257
pharmgkbrs180177257
gwascentralrs180177257
openSNPrs180177257
23andMers180177257
23andMe allrs180177257
SNP Nexus

SNPshotrs180177257
SNPdbers180177257
MSV3drs180177257
GWAS Ctlgrs180177257
Max Magnitude0
ClinVar
Risk rs180177257(T;T)
Alt rs180177257(T;T)
Reference rs180177257(;)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814570dupT
CLNSRC
CLNACC RCV000186404.1,