Have questions? Visit https://www.reddit.com/r/SNPedia

rs80356739

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356739(C;G)
Make rs80356739(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022545
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356739
ebirs80356739
HLIrs80356739
Exacrs80356739
Varsomers80356739
Maprs80356739
PheGenIrs80356739
hapmaprs80356739
1000 genomesrs80356739
hgdprs80356739
ensemblrs80356739
gopubmedrs80356739
geneviewrs80356739
scholarrs80356739
googlers80356739
pharmgkbrs80356739
gwascentralrs80356739
openSNPrs80356739
23andMers80356739
23andMe allrs80356739
SNP Nexus

SNPshotrs80356739
SNPdbers80356739
MSV3drs80356739
GWAS Ctlgrs80356739
Max Magnitude0
ClinVar
Risk rs80356739(G;G)
Alt rs80356739(G;G)
Reference rs80356739(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.11022545C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020662.1,