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rs61729604

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61729604(A;A)
Make rs61729604(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240877556
GeneAGXT
is asnp
is mentioned by
dbSNPrs61729604
ebirs61729604
HLIrs61729604
Exacrs61729604
Varsomers61729604
Maprs61729604
PheGenIrs61729604
hapmaprs61729604
1000 genomesrs61729604
hgdprs61729604
ensemblrs61729604
gopubmedrs61729604
geneviewrs61729604
scholarrs61729604
googlers61729604
pharmgkbrs61729604
gwascentralrs61729604
openSNPrs61729604
23andMers61729604
23andMe allrs61729604
SNP Nexus

SNPshotrs61729604
SNPdbers61729604
MSV3drs61729604
GWAS Ctlgrs61729604
Max Magnitude0
ClinVar
Risk rs61729604(A;A)
Alt rs61729604(A;A)
Reference rs61729604(G;G)
Significance Pathogenic
Disease not provided Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN not provided Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241816973G>A
CLNSRC
CLNACC RCV000180453.1, RCV000186341.1,