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rs180177229

From SNPedia

Merged intors180177227
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177229(G;T)
Make rs180177229(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240871406
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177229
ebirs180177229
HLIrs180177229
Exacrs180177229
Varsomers180177229
Maprs180177229
PheGenIrs180177229
hapmaprs180177229
1000 genomesrs180177229
hgdprs180177229
ensemblrs180177229
gopubmedrs180177229
geneviewrs180177229
scholarrs180177229
googlers180177229
pharmgkbrs180177229
gwascentralrs180177229
openSNPrs180177229
23andMers180177229
23andMe allrs180177229
SNP Nexus

SNPshotrs180177229
SNPdbers180177229
MSV3drs180177229
GWAS Ctlgrs180177229
StatusMerged into rs180177227
Max Magnitude0
ClinVar
Risk rs180177229(T;T)
Alt rs180177229(T;T)
Reference rs180177229(G;G)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241810823G>T
CLNSRC
CLNACC