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rs180177169

From SNPedia

Merged intors180177168
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177169(G;T)
Make rs180177169(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240868987
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177169
ebirs180177169
HLIrs180177169
Exacrs180177169
Varsomers180177169
Maprs180177169
PheGenIrs180177169
hapmaprs180177169
1000 genomesrs180177169
hgdprs180177169
ensemblrs180177169
gopubmedrs180177169
geneviewrs180177169
scholarrs180177169
googlers180177169
pharmgkbrs180177169
gwascentralrs180177169
openSNPrs180177169
23andMers180177169
23andMe allrs180177169
SNP Nexus

SNPshotrs180177169
SNPdbers180177169
MSV3drs180177169
GWAS Ctlgrs180177169
StatusMerged into rs180177168
Max Magnitude0
ClinVar
Risk rs180177169(T;T)
Alt rs180177169(T;T)
Reference rs180177169(G;G)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241808404G>T
CLNSRC
CLNACC