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rs180177156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177156(A;A)
Make rs180177156(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878128
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177156
dbSNP (old)rs180177156
ClinGenrs180177156
ebirs180177156
HLIrs180177156
Exacrs180177156
Gnomadrs180177156
Varsomers180177156
Maprs180177156
PheGenIrs180177156
Biobankrs180177156
1000 genomesrs180177156
hgdprs180177156
ensemblrs180177156
gopubmedrs180177156
geneviewrs180177156
scholarrs180177156
googlers180177156
pharmgkbrs180177156
gwascentralrs180177156
openSNPrs180177156
23andMers180177156
23andMe allrs180177156
SNP Nexus

SNPshotrs180177156
SNPdbers180177156
MSV3drs180177156
GWAS Ctlgrs180177156
Max Magnitude0
ClinVar
Risk rs180177156(A;A) rs180177156(T;T)
Alt rs180177156(A;A) rs180177156(T;T)
Reference Rs180177156(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817545G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000169365.2,