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rs876657406

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657406(C;C)
Make rs876657406(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position64498041
GeneTBK1
is asnp
is mentioned by
dbSNPrs876657406
ebirs876657406
HLIrs876657406
Exacrs876657406
Varsomers876657406
Maprs876657406
PheGenIrs876657406
hapmaprs876657406
1000 genomesrs876657406
hgdprs876657406
ensemblrs876657406
gopubmedrs876657406
geneviewrs876657406
scholarrs876657406
googlers876657406
pharmgkbrs876657406
gwascentralrs876657406
openSNPrs876657406
23andMers876657406
23andMe allrs876657406
SNP Nexus

SNPshotrs876657406
SNPdbers876657406
MSV3drs876657406
GWAS Ctlgrs876657406
Max Magnitude0
ClinVar
Risk rs876657406(C;C)
Alt rs876657406(C;C)
Reference rs876657406(T;T)
Significance Pathogenic
Disease Frontotemporal dementia and/or amyotrophic lateral sclerosis 4
Variation info
Gene TBK1
CLNDBN Frontotemporal dementia and/or amyotrophic lateral sclerosis 4
Reversed 0
HGVS NC_000012.11:g.64891821T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000185597.2,