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rs80356725

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80356725(A;G)
Make rs80356725(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022340
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356725
ebirs80356725
HLIrs80356725
Exacrs80356725
Varsomers80356725
Maprs80356725
PheGenIrs80356725
hapmaprs80356725
1000 genomesrs80356725
hgdprs80356725
ensemblrs80356725
gopubmedrs80356725
geneviewrs80356725
scholarrs80356725
googlers80356725
pharmgkbrs80356725
gwascentralrs80356725
openSNPrs80356725
23andMers80356725
23andMe allrs80356725
SNP Nexus

SNPshotrs80356725
SNPdbers80356725
MSV3drs80356725
GWAS Ctlgrs80356725
Max Magnitude0
ClinVar
Risk rs80356725(G;G)
Alt rs80356725(G;G)
Reference rs80356725(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.11022340A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020676.1,