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rs180177226

From SNPedia

Merged intors180177225
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs180177226(C;T)
Make rs180177226(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240871398
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177226
ebirs180177226
HLIrs180177226
Exacrs180177226
Varsomers180177226
Maprs180177226
PheGenIrs180177226
hapmaprs180177226
1000 genomesrs180177226
hgdprs180177226
ensemblrs180177226
gopubmedrs180177226
geneviewrs180177226
scholarrs180177226
googlers180177226
pharmgkbrs180177226
gwascentralrs180177226
openSNPrs180177226
23andMers180177226
23andMe allrs180177226
SNP Nexus

SNPshotrs180177226
SNPdbers180177226
MSV3drs180177226
GWAS Ctlgrs180177226
StatusMerged into rs180177225
Max Magnitude0
ClinVar
Risk rs180177226(T;T)
Alt rs180177226(T;T)
Reference rs180177226(C;C)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241810815C>T
CLNSRC
CLNACC