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rs796052067

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052067(G;T)
Make rs796052067(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240869363
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs796052067
ebirs796052067
HLIrs796052067
Exacrs796052067
Varsomers796052067
Maprs796052067
PheGenIrs796052067
hapmaprs796052067
1000 genomesrs796052067
hgdprs796052067
ensemblrs796052067
gopubmedrs796052067
geneviewrs796052067
scholarrs796052067
googlers796052067
pharmgkbrs796052067
gwascentralrs796052067
openSNPrs796052067
23andMers796052067
23andMe allrs796052067
SNP Nexus

SNPshotrs796052067
SNPdbers796052067
MSV3drs796052067
GWAS Ctlgrs796052067
Max Magnitude0
ClinVar
Risk rs796052067(T;T)
Alt rs796052067(T;T)
Reference rs796052067(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808780G>T
CLNSRC
CLNACC RCV000186358.1,