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rs180177205

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177205(-;-)
Make rs180177205(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868898
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177205
ebirs180177205
HLIrs180177205
Exacrs180177205
Varsomers180177205
Maprs180177205
PheGenIrs180177205
hapmaprs180177205
1000 genomesrs180177205
hgdprs180177205
ensemblrs180177205
gopubmedrs180177205
geneviewrs180177205
scholarrs180177205
googlers180177205
pharmgkbrs180177205
gwascentralrs180177205
openSNPrs180177205
23andMers180177205
23andMe allrs180177205
SNP Nexus

SNPshotrs180177205
SNPdbers180177205
MSV3drs180177205
GWAS Ctlgrs180177205
Max Magnitude0
ClinVar
Risk rs180177205(;)
Alt rs180177205(;)
Reference rs180177205(C;C)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808315delC
CLNSRC
CLNACC RCV000169102.2,