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rs767586362

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767586362(A;A)
Make rs767586362(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240869179
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs767586362
ebirs767586362
HLIrs767586362
Exacrs767586362
Varsomers767586362
Maprs767586362
PheGenIrs767586362
hapmaprs767586362
1000 genomesrs767586362
hgdprs767586362
ensemblrs767586362
gopubmedrs767586362
geneviewrs767586362
scholarrs767586362
googlers767586362
pharmgkbrs767586362
gwascentralrs767586362
openSNPrs767586362
23andMers767586362
23andMe allrs767586362
SNP Nexus

SNPshotrs767586362
SNPdbers767586362
MSV3drs767586362
GWAS Ctlgrs767586362
Max Magnitude0
ClinVar
Risk rs767586362(A;A)
Alt rs767586362(A;A)
Reference rs767586362(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808596G>A
CLNSRC
CLNACC RCV000186284.1,