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rs180177207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177207(A;A)
Make rs180177207(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240869350
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177207
ebirs180177207
HLIrs180177207
Exacrs180177207
Varsomers180177207
Maprs180177207
PheGenIrs180177207
hapmaprs180177207
1000 genomesrs180177207
hgdprs180177207
ensemblrs180177207
gopubmedrs180177207
geneviewrs180177207
scholarrs180177207
googlers180177207
pharmgkbrs180177207
gwascentralrs180177207
openSNPrs180177207
23andMers180177207
23andMe allrs180177207
SNP Nexus

SNPshotrs180177207
SNPdbers180177207
MSV3drs180177207
GWAS Ctlgrs180177207
Max Magnitude0
ClinVar
Risk rs180177207(A;A)
Alt rs180177207(A;A)
Reference rs180177207(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808767G>A
CLNSRC
CLNACC RCV000169408.2,