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rs80356718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356718(A;G)
Make rs80356718(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022209
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356718
ebirs80356718
HLIrs80356718
Exacrs80356718
Varsomers80356718
Maprs80356718
PheGenIrs80356718
hapmaprs80356718
1000 genomesrs80356718
hgdprs80356718
ensemblrs80356718
gopubmedrs80356718
geneviewrs80356718
scholarrs80356718
googlers80356718
pharmgkbrs80356718
gwascentralrs80356718
openSNPrs80356718
23andMers80356718
23andMe allrs80356718
SNP Nexus

SNPshotrs80356718
SNPdbers80356718
MSV3drs80356718
GWAS Ctlgrs80356718
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs80356718(G;G)
Alt rs80356718(G;G)
Reference rs80356718(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.11022209A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020671.1,