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rs80356741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356741(A;G)
Make rs80356741(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022577
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356741
ebirs80356741
HLIrs80356741
Exacrs80356741
Varsomers80356741
Maprs80356741
PheGenIrs80356741
hapmaprs80356741
1000 genomesrs80356741
hgdprs80356741
ensemblrs80356741
gopubmedrs80356741
geneviewrs80356741
scholarrs80356741
googlers80356741
pharmgkbrs80356741
gwascentralrs80356741
openSNPrs80356741
23andMers80356741
23andMe allrs80356741
SNP Nexus

SNPshotrs80356741
SNPdbers80356741
MSV3drs80356741
GWAS Ctlgrs80356741
Max Magnitude0
ClinVar
Risk rs80356741(G;G)
Alt rs80356741(G;G)
Reference rs80356741(A;A)
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.11022577A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020666.1,