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rs180177301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177301(-;-)
Make rs180177301(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878055
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177301
ebirs180177301
HLIrs180177301
Exacrs180177301
Varsomers180177301
Maprs180177301
PheGenIrs180177301
hapmaprs180177301
1000 genomesrs180177301
hgdprs180177301
ensemblrs180177301
gopubmedrs180177301
geneviewrs180177301
scholarrs180177301
googlers180177301
pharmgkbrs180177301
gwascentralrs180177301
openSNPrs180177301
23andMers180177301
23andMe allrs180177301
SNP Nexus

SNPshotrs180177301
SNPdbers180177301
MSV3drs180177301
GWAS Ctlgrs180177301
Max Magnitude0
ClinVar
Risk rs180177301(;)
Alt rs180177301(;)
Reference rs180177301(G;G)
Significance Other
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817472delG
CLNSRC
CLNACC RCV000169587.2,