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rs147810437

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs147810437(C;T)
Make rs147810437(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position179823906
GeneSQSTM1
is asnp
is mentioned by
dbSNPrs147810437
ebirs147810437
HLIrs147810437
Exacrs147810437
Varsomers147810437
Maprs147810437
PheGenIrs147810437
hapmaprs147810437
1000 genomesrs147810437
hgdprs147810437
ensemblrs147810437
gopubmedrs147810437
geneviewrs147810437
scholarrs147810437
googlers147810437
pharmgkbrs147810437
gwascentralrs147810437
openSNPrs147810437
23andMers147810437
23andMe allrs147810437
SNP Nexus

SNPshotrs147810437
SNPdbers147810437
MSV3drs147810437
GWAS Ctlgrs147810437
Max Magnitude0
ClinVar
Risk rs147810437(T;T)
Alt rs147810437(T;T)
Reference rs147810437(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.179250906C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000184066.3,