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

rs80356740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356740(A;G)
Make rs80356740(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022556
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356740
ebirs80356740
HLIrs80356740
Exacrs80356740
Varsomers80356740
Maprs80356740
PheGenIrs80356740
hapmaprs80356740
1000 genomesrs80356740
hgdprs80356740
ensemblrs80356740
gopubmedrs80356740
geneviewrs80356740
scholarrs80356740
googlers80356740
pharmgkbrs80356740
gwascentralrs80356740
openSNPrs80356740
23andMers80356740
23andMe allrs80356740
SNP Nexus

SNPshotrs80356740
SNPdbers80356740
MSV3drs80356740
GWAS Ctlgrs80356740
Max Magnitude0
ClinVar
Risk rs80356740(G;G)
Alt rs80356740(G;G)
Reference rs80356740(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.11022556A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020665.1,