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rs13036957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs13036957(A;A)
Make rs13036957(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position43193056
is asnp
is mentioned by
dbSNPrs13036957
dbSNP (classic)rs13036957
ClinGenrs13036957
ebirs13036957
HLIrs13036957
Exacrs13036957
Gnomadrs13036957
Varsomers13036957
LitVarrs13036957
Maprs13036957
PheGenIrs13036957
Biobankrs13036957
1000 genomesrs13036957
hgdprs13036957
ensemblrs13036957
geneviewrs13036957
scholarrs13036957
googlers13036957
pharmgkbrs13036957
gwascentralrs13036957
openSNPrs13036957
23andMers13036957
SNPshotrs13036957
SNPdbers13036957
MSV3drs13036957
GWAS Ctlgrs13036957
GMAF0.1956
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]