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rs113681235

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs113681235(G;G)
Make rs113681235(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869364
GeneAGXT
is asnp
is mentioned by
dbSNPrs113681235
ebirs113681235
HLIrs113681235
Exacrs113681235
Varsomers113681235
Maprs113681235
PheGenIrs113681235
hapmaprs113681235
1000 genomesrs113681235
hgdprs113681235
ensemblrs113681235
gopubmedrs113681235
geneviewrs113681235
scholarrs113681235
googlers113681235
pharmgkbrs113681235
gwascentralrs113681235
openSNPrs113681235
23andMers113681235
23andMe allrs113681235
SNP Nexus

SNPshotrs113681235
SNPdbers113681235
MSV3drs113681235
GWAS Ctlgrs113681235
Max Magnitude0
ClinVar
Risk rs113681235(A,G;A,G)
Alt rs113681235(A,G;A,G)
Reference rs113681235(T;T)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808781T>G
CLNSRC
CLNACC RCV000186359.1,


OMIM259900
Desc
Variant
Relatedalso