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rs180177275

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs180177275(-;-)
Make rs180177275(-;A)
Make rs180177275(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position240875987
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177275
ebirs180177275
HLIrs180177275
Exacrs180177275
Varsomers180177275
Maprs180177275
PheGenIrs180177275
hapmaprs180177275
1000 genomesrs180177275
hgdprs180177275
ensemblrs180177275
gopubmedrs180177275
geneviewrs180177275
scholarrs180177275
googlers180177275
pharmgkbrs180177275
gwascentralrs180177275
openSNPrs180177275
23andMers180177275
23andMe allrs180177275
SNP Nexus

SNPshotrs180177275
SNPdbers180177275
MSV3drs180177275
GWAS Ctlgrs180177275
Max Magnitude0
ClinVar
Risk rs180177275(A;A)
Alt rs180177275(A;A)
Reference rs180177275(;)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241815404_241815405insA
CLNSRC
CLNACC RCV000186409.1,