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

rs180177203

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177203(A;A)
Make rs180177203(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240869336
GeneAGXT, LOC105373969
is asnp
is mentioned by
dbSNPrs180177203
ebirs180177203
HLIrs180177203
Exacrs180177203
Varsomers180177203
Maprs180177203
PheGenIrs180177203
hapmaprs180177203
1000 genomesrs180177203
hgdprs180177203
ensemblrs180177203
gopubmedrs180177203
geneviewrs180177203
scholarrs180177203
googlers180177203
pharmgkbrs180177203
gwascentralrs180177203
openSNPrs180177203
23andMers180177203
23andMe allrs180177203
SNP Nexus

SNPshotrs180177203
SNPdbers180177203
MSV3drs180177203
GWAS Ctlgrs180177203
Max Magnitude0
ClinVar
Risk rs180177203(A,T;A,T)
Alt rs180177203(A,T;A,T)
Reference rs180177203(G;G)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241808753G>A
CLNSRC
CLNACC RCV000186298.1,