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rs180177195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs180177195(C;C)
Make rs180177195(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869306
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177195
ebirs180177195
HLIrs180177195
Exacrs180177195
Varsomers180177195
Maprs180177195
PheGenIrs180177195
hapmaprs180177195
1000 genomesrs180177195
hgdprs180177195
ensemblrs180177195
gopubmedrs180177195
geneviewrs180177195
scholarrs180177195
googlers180177195
pharmgkbrs180177195
gwascentralrs180177195
openSNPrs180177195
23andMers180177195
23andMe allrs180177195
SNP Nexus

SNPshotrs180177195
SNPdbers180177195
MSV3drs180177195
GWAS Ctlgrs180177195
Max Magnitude0
ClinVar
Risk rs180177195(C;C)
Alt rs180177195(C;C)
Reference rs180177195(T;T)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808723T>C
CLNSRC
CLNACC RCV000169219.2,