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rs776749939

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776749939(C;T)
Make rs776749939(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position179833777
GeneSQSTM1
is asnp
is mentioned by
dbSNPrs776749939
ebirs776749939
HLIrs776749939
Exacrs776749939
Varsomers776749939
Maprs776749939
PheGenIrs776749939
hapmaprs776749939
1000 genomesrs776749939
hgdprs776749939
ensemblrs776749939
gopubmedrs776749939
geneviewrs776749939
scholarrs776749939
googlers776749939
pharmgkbrs776749939
gwascentralrs776749939
openSNPrs776749939
23andMers776749939
23andMe allrs776749939
SNP Nexus

SNPshotrs776749939
SNPdbers776749939
MSV3drs776749939
GWAS Ctlgrs776749939
Max Magnitude0
ClinVar
Risk rs776749939(T;T)
Alt rs776749939(T;T)
Reference rs776749939(C;C)
Significance Pathogenic
Disease Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Variation info
Gene SQSTM1
CLNDBN Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Reversed 0
HGVS NC_000005.9:g.179260777C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000184065.2,