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

rs80356742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356742(A;G)
Make rs80356742(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022578
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356742
ebirs80356742
HLIrs80356742
Exacrs80356742
Varsomers80356742
Maprs80356742
PheGenIrs80356742
hapmaprs80356742
1000 genomesrs80356742
hgdprs80356742
ensemblrs80356742
gopubmedrs80356742
geneviewrs80356742
scholarrs80356742
googlers80356742
pharmgkbrs80356742
gwascentralrs80356742
openSNPrs80356742
23andMers80356742
23andMe allrs80356742
SNP Nexus

SNPshotrs80356742
SNPdbers80356742
MSV3drs80356742
GWAS Ctlgrs80356742
Max Magnitude0
ClinVar
Risk rs80356742(G;G)
Alt rs80356742(G;G)
Reference rs80356742(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.11022578A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020667.1,