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rs180177273

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs180177273(-;-)
Make rs180177273(-;AG)
Make rs180177273(AG;AG)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875982
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177273
ebirs180177273
HLIrs180177273
Exacrs180177273
Varsomers180177273
Maprs180177273
PheGenIrs180177273
hapmaprs180177273
1000 genomesrs180177273
hgdprs180177273
ensemblrs180177273
gopubmedrs180177273
geneviewrs180177273
scholarrs180177273
googlers180177273
pharmgkbrs180177273
gwascentralrs180177273
openSNPrs180177273
23andMers180177273
23andMe allrs180177273
SNP Nexus

SNPshotrs180177273
SNPdbers180177273
MSV3drs180177273
GWAS Ctlgrs180177273
Max Magnitude0
ClinVar
Risk rs180177273(GA;GA)
Alt rs180177273(GA;GA)
Reference rs180177273(;)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815398_241815399dupAG
CLNSRC
CLNACC RCV000186408.1,