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

rs180177243

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177243(A;C)
Make rs180177243(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position240873037
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177243
ebirs180177243
HLIrs180177243
Exacrs180177243
Varsomers180177243
Maprs180177243
PheGenIrs180177243
hapmaprs180177243
1000 genomesrs180177243
hgdprs180177243
ensemblrs180177243
gopubmedrs180177243
geneviewrs180177243
scholarrs180177243
googlers180177243
pharmgkbrs180177243
gwascentralrs180177243
openSNPrs180177243
23andMers180177243
23andMe allrs180177243
SNP Nexus

SNPshotrs180177243
SNPdbers180177243
MSV3drs180177243
GWAS Ctlgrs180177243
Max Magnitude0
ClinVar
Risk rs180177243(C,G;C,G)
Alt rs180177243(C,G;C,G)
Reference rs180177243(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241812454A>C
CLNSRC
CLNACC RCV000186318.1,