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rs767898276

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767898276(A;A)
Make rs767898276(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position64486018
GeneTBK1
is asnp
is mentioned by
dbSNPrs767898276
ebirs767898276
HLIrs767898276
Exacrs767898276
Varsomers767898276
Maprs767898276
PheGenIrs767898276
hapmaprs767898276
1000 genomesrs767898276
hgdprs767898276
ensemblrs767898276
gopubmedrs767898276
geneviewrs767898276
scholarrs767898276
googlers767898276
pharmgkbrs767898276
gwascentralrs767898276
openSNPrs767898276
23andMers767898276
23andMe allrs767898276
SNP Nexus

SNPshotrs767898276
SNPdbers767898276
MSV3drs767898276
GWAS Ctlgrs767898276
Max Magnitude0
ClinVar
Risk rs767898276(A;A)
Alt rs767898276(A;A)
Reference rs767898276(G;G)
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.64879798G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000185599.2,