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rs80356719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356719(A;A)
Make rs80356719(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022268
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356719
ebirs80356719
HLIrs80356719
Exacrs80356719
Varsomers80356719
Maprs80356719
PheGenIrs80356719
hapmaprs80356719
1000 genomesrs80356719
hgdprs80356719
ensemblrs80356719
gopubmedrs80356719
geneviewrs80356719
scholarrs80356719
googlers80356719
pharmgkbrs80356719
gwascentralrs80356719
openSNPrs80356719
23andMers80356719
23andMe allrs80356719
SNP Nexus

SNPshotrs80356719
SNPdbers80356719
MSV3drs80356719
GWAS Ctlgrs80356719
Max Magnitude0
ClinVar
Risk rs80356719(A,C;A,C)
Alt rs80356719(A,C;A,C)
Reference rs80356719(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.11022268G>A; NC_000001.11:g.11022268G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000020672.1, RCV000032100.1,


[PMID 18396105OA-icon.png] TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.