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rs80356727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356727(A;A)
Make rs80356727(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022400
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356727
ebirs80356727
HLIrs80356727
Exacrs80356727
Varsomers80356727
Maprs80356727
PheGenIrs80356727
hapmaprs80356727
1000 genomesrs80356727
hgdprs80356727
ensemblrs80356727
gopubmedrs80356727
geneviewrs80356727
scholarrs80356727
googlers80356727
pharmgkbrs80356727
gwascentralrs80356727
openSNPrs80356727
23andMers80356727
23andMe allrs80356727
SNP Nexus

SNPshotrs80356727
SNPdbers80356727
MSV3drs80356727
GWAS Ctlgrs80356727
Max Magnitude0
OMIM605078
Desc
Variant0002
Relatedalso
ClinVar
Risk rs80356727(A;A)
Alt rs80356727(A;A)
Reference rs80356727(C;C)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 10
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10
Reversed 0
HGVS NC_000001.10:g.11082457C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005540.3,