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rs387906334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906334(A;A)
Make rs387906334(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position11023351
GeneTARDBP
is asnp
is mentioned by
dbSNPrs387906334
ebirs387906334
HLIrs387906334
Exacrs387906334
Varsomers387906334
Maprs387906334
PheGenIrs387906334
hapmaprs387906334
1000 genomesrs387906334
hgdprs387906334
ensemblrs387906334
gopubmedrs387906334
geneviewrs387906334
scholarrs387906334
googlers387906334
pharmgkbrs387906334
gwascentralrs387906334
openSNPrs387906334
23andMers387906334
23andMe allrs387906334
SNP Nexus

SNPshotrs387906334
SNPdbers387906334
MSV3drs387906334
GWAS Ctlgrs387906334
Max Magnitude0
ClinVar
Risk rs387906334(A;A)
Alt rs387906334(A;A)
Reference rs387906334(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 10 FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10 FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
Reversed 0
HGVS NC_000001.10:g.11083408G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005550.2, RCV000005551.2,