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rs80356729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356729(A;A)
Make rs80356729(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022413
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356729
ebirs80356729
HLIrs80356729
Exacrs80356729
Varsomers80356729
Maprs80356729
PheGenIrs80356729
hapmaprs80356729
1000 genomesrs80356729
hgdprs80356729
ensemblrs80356729
gopubmedrs80356729
geneviewrs80356729
scholarrs80356729
googlers80356729
pharmgkbrs80356729
gwascentralrs80356729
openSNPrs80356729
23andMers80356729
23andMe allrs80356729
SNP Nexus

SNPshotrs80356729
SNPdbers80356729
MSV3drs80356729
GWAS Ctlgrs80356729
Max Magnitude0
ClinVar
Risk rs80356729(A;A)
Alt rs80356729(A;A)
Reference rs80356729(G;G)
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.11022413G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020655.1,