Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177303

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177303(A;T)
Make rs180177303(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240878076
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177303
ebirs180177303
HLIrs180177303
Exacrs180177303
Varsomers180177303
Maprs180177303
PheGenIrs180177303
hapmaprs180177303
1000 genomesrs180177303
hgdprs180177303
ensemblrs180177303
gopubmedrs180177303
geneviewrs180177303
scholarrs180177303
googlers180177303
pharmgkbrs180177303
gwascentralrs180177303
openSNPrs180177303
23andMers180177303
23andMe allrs180177303
SNP Nexus

SNPshotrs180177303
SNPdbers180177303
MSV3drs180177303
GWAS Ctlgrs180177303
Max Magnitude0
ClinVar
Risk rs180177303(T;T)
Alt rs180177303(T;T)
Reference rs180177303(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241817493A>T
CLNSRC
CLNACC RCV000186349.1,