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rs180177166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
Make rs180177166(-;CA)
Make rs180177166(CA;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868982
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177166
ebirs180177166
HLIrs180177166
Exacrs180177166
Varsomers180177166
Maprs180177166
PheGenIrs180177166
hapmaprs180177166
1000 genomesrs180177166
hgdprs180177166
ensemblrs180177166
gopubmedrs180177166
geneviewrs180177166
scholarrs180177166
googlers180177166
pharmgkbrs180177166
gwascentralrs180177166
openSNPrs180177166
23andMers180177166
23andMe allrs180177166
SNP Nexus

SNPshotrs180177166
SNPdbers180177166
MSV3drs180177166
GWAS Ctlgrs180177166
Max Magnitude0
ClinVar
Risk rs180177166(CA;CA)
Alt rs180177166(CA;CA)
Reference rs180177166(;)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808398_241808399dupCA
CLNSRC
CLNACC RCV000186382.1,