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rs1027615

From SNPedia

Orientationplus
Stabilizedplus
Make rs1027615(A;A)
Make rs1027615(A;G)
Make rs1027615(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position43318486
is asnp
is mentioned by
dbSNPrs1027615
dbSNP (classic)rs1027615
ClinGenrs1027615
ebirs1027615
HLIrs1027615
Exacrs1027615
Gnomadrs1027615
Varsomers1027615
LitVarrs1027615
Maprs1027615
PheGenIrs1027615
Biobankrs1027615
1000 genomesrs1027615
hgdprs1027615
ensemblrs1027615
geneviewrs1027615
scholarrs1027615
googlers1027615
pharmgkbrs1027615
gwascentralrs1027615
openSNPrs1027615
23andMers1027615
SNPshotrs1027615
SNPdbers1027615
MSV3drs1027615
GWAS Ctlgrs1027615
GMAF0.168
Max Magnitude0
? (A;A) (A;G) (G;G) 28


This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]