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rs80356728

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356728(A;A)
Make rs80356728(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11022404
GeneTARDBP
is asnp
is mentioned by
dbSNPrs80356728
ebirs80356728
HLIrs80356728
Exacrs80356728
Varsomers80356728
Maprs80356728
PheGenIrs80356728
hapmaprs80356728
1000 genomesrs80356728
hgdprs80356728
ensemblrs80356728
gopubmedrs80356728
geneviewrs80356728
scholarrs80356728
googlers80356728
pharmgkbrs80356728
gwascentralrs80356728
openSNPrs80356728
23andMers80356728
23andMe allrs80356728
SNP Nexus

SNPshotrs80356728
SNPdbers80356728
MSV3drs80356728
GWAS Ctlgrs80356728
Max Magnitude0
ClinVar
Risk rs80356728(A;A)
Alt rs80356728(A;A)
Reference rs80356728(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.11022404G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020677.1,