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

rs80356734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356734(A;G)
Make rs80356734(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022464
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356734
ebirs80356734
HLIrs80356734
Exacrs80356734
Varsomers80356734
Maprs80356734
PheGenIrs80356734
hapmaprs80356734
1000 genomesrs80356734
hgdprs80356734
ensemblrs80356734
gopubmedrs80356734
geneviewrs80356734
scholarrs80356734
googlers80356734
pharmgkbrs80356734
gwascentralrs80356734
openSNPrs80356734
23andMers80356734
23andMe allrs80356734
SNP Nexus

SNPshotrs80356734
SNPdbers80356734
MSV3drs80356734
GWAS Ctlgrs80356734
Max Magnitude0
ClinVar
Risk rs80356734(G;G)
Alt rs80356734(G;G)
Reference rs80356734(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.11022464A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020657.1,