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rs80356736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356736(C;G)
Make rs80356736(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022506
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356736
ebirs80356736
HLIrs80356736
Exacrs80356736
Varsomers80356736
Maprs80356736
PheGenIrs80356736
hapmaprs80356736
1000 genomesrs80356736
hgdprs80356736
ensemblrs80356736
gopubmedrs80356736
geneviewrs80356736
scholarrs80356736
googlers80356736
pharmgkbrs80356736
gwascentralrs80356736
openSNPrs80356736
23andMers80356736
23andMe allrs80356736
SNP Nexus

SNPshotrs80356736
SNPdbers80356736
MSV3drs80356736
GWAS Ctlgrs80356736
Max Magnitude0
ClinVar
Risk rs80356736(G;G)
Alt rs80356736(G;G)
Reference rs80356736(C;C)
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.11022506C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020659.1,