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rs797044594

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044594(C;C)
Make rs797044594(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11022559
GeneTARDBP
is asnp
is mentioned by
dbSNPrs797044594
ebirs797044594
HLIrs797044594
Exacrs797044594
Varsomers797044594
Maprs797044594
PheGenIrs797044594
hapmaprs797044594
1000 genomesrs797044594
hgdprs797044594
ensemblrs797044594
gopubmedrs797044594
geneviewrs797044594
scholarrs797044594
googlers797044594
pharmgkbrs797044594
gwascentralrs797044594
openSNPrs797044594
23andMers797044594
23andMe allrs797044594
SNP Nexus

SNPshotrs797044594
SNPdbers797044594
MSV3drs797044594
GWAS Ctlgrs797044594
Max Magnitude0
ClinVar
Risk rs797044594(C;C)
Alt rs797044594(C;C)
Reference rs797044594(G;G)
Significance Pathogenic
Disease Amyotrophic lateral sclerosis type 10
Variation info
Gene TARDBP
CLNDBN Amyotrophic lateral sclerosis type 10
Reversed 0
HGVS NC_000001.10:g.11082616G>C
CLNSRC
CLNACC RCV000192195.1,