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rs80356738

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80356738(C;C)
Make rs80356738(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022544
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356738
ebirs80356738
HLIrs80356738
Exacrs80356738
Varsomers80356738
Maprs80356738
PheGenIrs80356738
hapmaprs80356738
1000 genomesrs80356738
hgdprs80356738
ensemblrs80356738
gopubmedrs80356738
geneviewrs80356738
scholarrs80356738
googlers80356738
pharmgkbrs80356738
gwascentralrs80356738
openSNPrs80356738
23andMers80356738
23andMe allrs80356738
SNP Nexus

SNPshotrs80356738
SNPdbers80356738
MSV3drs80356738
GWAS Ctlgrs80356738
Max Magnitude0
ClinVar
Risk rs80356738(C;C)
Alt rs80356738(C;C)
Reference rs80356738(T;T)
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.11022544T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000020661.1,