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rs80356737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(TAT;TAT) 0 common in clinvar
Make rs80356737(-;-)
Make rs80356737(-;A)
Make rs80356737(A;A)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022530
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356737
ebirs80356737
HLIrs80356737
Exacrs80356737
Varsomers80356737
Maprs80356737
PheGenIrs80356737
hapmaprs80356737
1000 genomesrs80356737
hgdprs80356737
ensemblrs80356737
gopubmedrs80356737
geneviewrs80356737
scholarrs80356737
googlers80356737
pharmgkbrs80356737
gwascentralrs80356737
openSNPrs80356737
23andMers80356737
23andMe allrs80356737
SNP Nexus

SNPshotrs80356737
SNPdbers80356737
MSV3drs80356737
GWAS Ctlgrs80356737
Max Magnitude0
ClinVar
Risk rs80356737(A;A)
Alt rs80356737(A;A)
Reference rs80356737(TAT;TAT)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 10
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10
Reversed 0
HGVS NC_000001.11:g.11022530dupA
CLNSRC ClinVar GeneReviews
CLNACC RCV000020660.1,


[PMID 18931000] Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.