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rs80356735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356735(G;T)
Make rs80356735(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022492
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356735
ebirs80356735
HLIrs80356735
Exacrs80356735
Varsomers80356735
Maprs80356735
PheGenIrs80356735
hapmaprs80356735
1000 genomesrs80356735
hgdprs80356735
ensemblrs80356735
gopubmedrs80356735
geneviewrs80356735
scholarrs80356735
googlers80356735
pharmgkbrs80356735
gwascentralrs80356735
openSNPrs80356735
23andMers80356735
23andMe allrs80356735
SNP Nexus

SNPshotrs80356735
SNPdbers80356735
MSV3drs80356735
GWAS Ctlgrs80356735
Max Magnitude0
ClinVar
Risk rs80356735(T;T)
Alt rs80356735(T;T)
Reference rs80356735(G;G)
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.11022492G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020658.1,