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rs180177180

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177180(A;A)
Make rs180177180(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240869171
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs180177180
ebirs180177180
HLIrs180177180
Exacrs180177180
Varsomers180177180
Maprs180177180
PheGenIrs180177180
hapmaprs180177180
1000 genomesrs180177180
hgdprs180177180
ensemblrs180177180
gopubmedrs180177180
geneviewrs180177180
scholarrs180177180
googlers180177180
pharmgkbrs180177180
gwascentralrs180177180
openSNPrs180177180
23andMers180177180
23andMe allrs180177180
SNP Nexus

SNPshotrs180177180
SNPdbers180177180
MSV3drs180177180
GWAS Ctlgrs180177180
Max Magnitude0
ClinVar
Risk rs180177180(A;A)
Alt rs180177180(A;A)
Reference rs180177180(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808588T>A
CLNSRC
CLNACC RCV000186283.1,