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rs80356716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80356716(A;A)
Make rs80356716(A;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11013922
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356716
ebirs80356716
HLIrs80356716
Exacrs80356716
Varsomers80356716
Maprs80356716
PheGenIrs80356716
hapmaprs80356716
1000 genomesrs80356716
hgdprs80356716
ensemblrs80356716
gopubmedrs80356716
geneviewrs80356716
scholarrs80356716
googlers80356716
pharmgkbrs80356716
gwascentralrs80356716
openSNPrs80356716
23andMers80356716
23andMe allrs80356716
SNP Nexus

SNPshotrs80356716
SNPdbers80356716
MSV3drs80356716
GWAS Ctlgrs80356716
Max Magnitude0
ClinVar
Risk rs80356716(A;A)
Alt rs80356716(A;A)
Reference rs80356716(T;T)
Significance Non-pathogenic
Disease Amyotrophic lateral sclerosis type 10
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10
Reversed 0
HGVS NC_000001.11:g.11013922T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020669.1,


[PMID 18545701OA-icon.png] TDP-43 is not a common cause of sporadic amyotrophic lateral sclerosis.