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rs80356732

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356732(A;A)
Make rs80356732(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022444
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356732
ebirs80356732
HLIrs80356732
Exacrs80356732
Varsomers80356732
Maprs80356732
PheGenIrs80356732
hapmaprs80356732
1000 genomesrs80356732
hgdprs80356732
ensemblrs80356732
gopubmedrs80356732
geneviewrs80356732
scholarrs80356732
googlers80356732
pharmgkbrs80356732
gwascentralrs80356732
openSNPrs80356732
23andMers80356732
23andMe allrs80356732
SNP Nexus

SNPshotrs80356732
SNPdbers80356732
MSV3drs80356732
GWAS Ctlgrs80356732
Max Magnitude0
ClinVar
Risk rs80356732(A;A)
Alt rs80356732(A;A)
Reference rs80356732(C;C)
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.11022444C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020656.1,