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rs180177168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177168(A;A)
Make rs180177168(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868987
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177168
ebirs180177168
HLIrs180177168
Exacrs180177168
Varsomers180177168
Maprs180177168
PheGenIrs180177168
hapmaprs180177168
1000 genomesrs180177168
hgdprs180177168
ensemblrs180177168
gopubmedrs180177168
geneviewrs180177168
scholarrs180177168
googlers180177168
pharmgkbrs180177168
gwascentralrs180177168
openSNPrs180177168
23andMers180177168
23andMe allrs180177168
SNP Nexus

SNPshotrs180177168
SNPdbers180177168
MSV3drs180177168
GWAS Ctlgrs180177168
Merged fromRs180177169
Max Magnitude0
ClinVar
Risk rs180177168(A,T;A,T)
Alt rs180177168(A,T;A,T)
Reference rs180177168(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808404G>A; NC_000002.11:g.241808404G>T
CLNSRC
CLNACC RCV000186279.1, RCV000169364.2,