Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177259

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177259(A;A)
Make rs180177259(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875165
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177259
ebirs180177259
HLIrs180177259
Exacrs180177259
Varsomers180177259
Maprs180177259
PheGenIrs180177259
hapmaprs180177259
1000 genomesrs180177259
hgdprs180177259
ensemblrs180177259
gopubmedrs180177259
geneviewrs180177259
scholarrs180177259
googlers180177259
pharmgkbrs180177259
gwascentralrs180177259
openSNPrs180177259
23andMers180177259
23andMe allrs180177259
SNP Nexus

SNPshotrs180177259
SNPdbers180177259
MSV3drs180177259
GWAS Ctlgrs180177259
Max Magnitude0
ClinVar
Risk rs180177259(A;A)
Alt rs180177259(A;A)
Reference rs180177259(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241814582G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000169425.2,