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rs180177224

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs180177224(-;-)
Make rs180177224(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position240871385
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177224
ebirs180177224
HLIrs180177224
Exacrs180177224
Varsomers180177224
Maprs180177224
PheGenIrs180177224
hapmaprs180177224
1000 genomesrs180177224
hgdprs180177224
ensemblrs180177224
gopubmedrs180177224
geneviewrs180177224
scholarrs180177224
googlers180177224
pharmgkbrs180177224
gwascentralrs180177224
openSNPrs180177224
23andMers180177224
23andMe allrs180177224
SNP Nexus

SNPshotrs180177224
SNPdbers180177224
MSV3drs180177224
GWAS Ctlgrs180177224
Max Magnitude0
ClinVar
Risk rs180177224(;)
Alt rs180177224(;)
Reference rs180177224(A;A)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene AGXT
CLNDBN Primary hyperoxaluria, type I
Reversed 0
HGVS NC_000002.11:g.241810802delA
CLNSRC
CLNACC RCV000186394.1,