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rs180177282

From SNPedia

Merged intors180177281
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs180177282(G;T)
Make rs180177282(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position240876005
GeneAGXT
is asnp
is mentioned by
dbSNPrs180177282
ebirs180177282
HLIrs180177282
Exacrs180177282
Varsomers180177282
Maprs180177282
PheGenIrs180177282
hapmaprs180177282
1000 genomesrs180177282
hgdprs180177282
ensemblrs180177282
gopubmedrs180177282
geneviewrs180177282
scholarrs180177282
googlers180177282
pharmgkbrs180177282
gwascentralrs180177282
openSNPrs180177282
23andMers180177282
23andMe allrs180177282
SNP Nexus

SNPshotrs180177282
SNPdbers180177282
MSV3drs180177282
GWAS Ctlgrs180177282
StatusMerged into rs180177281
Max Magnitude0
ClinVar
Risk rs180177282(T;T)
Alt rs180177282(T;T)
Reference rs180177282(G;G)
Significance Pathogenic
Disease
Variation info
Gene AGXT
CLNDBN OMIM
Reversed 0
HGVS NC_000002.11:g.241815422G>T
CLNSRC
CLNACC