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rs797044595

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797044595(G;G)
Make rs797044595(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11022562
GeneTARDBP
is asnp
is mentioned by
dbSNPrs797044595
ebirs797044595
HLIrs797044595
Exacrs797044595
Varsomers797044595
Maprs797044595
PheGenIrs797044595
hapmaprs797044595
1000 genomesrs797044595
hgdprs797044595
ensemblrs797044595
gopubmedrs797044595
geneviewrs797044595
scholarrs797044595
googlers797044595
pharmgkbrs797044595
gwascentralrs797044595
openSNPrs797044595
23andMers797044595
23andMe allrs797044595
SNP Nexus

SNPshotrs797044595
SNPdbers797044595
MSV3drs797044595
GWAS Ctlgrs797044595
Max Magnitude0
ClinVar
Risk rs797044595(G;G)
Alt rs797044595(G;G)
Reference rs797044595(T;T)
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.11082619T>G
CLNSRC
CLNACC RCV000192196.1,