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rs796052214

From SNPedia

Orientationplus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs796052214(-;-)
Make rs796052214(-;GAA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position179825186
GeneSQSTM1
is asnp
is mentioned by
dbSNPrs796052214
ebirs796052214
HLIrs796052214
Exacrs796052214
Varsomers796052214
Maprs796052214
PheGenIrs796052214
hapmaprs796052214
1000 genomesrs796052214
hgdprs796052214
ensemblrs796052214
gopubmedrs796052214
geneviewrs796052214
scholarrs796052214
googlers796052214
pharmgkbrs796052214
gwascentralrs796052214
openSNPrs796052214
23andMers796052214
23andMe allrs796052214
SNP Nexus

SNPshotrs796052214
SNPdbers796052214
MSV3drs796052214
GWAS Ctlgrs796052214
Max Magnitude0
ClinVar
Risk rs796052214(;)
Alt rs796052214(;)
Reference rs796052214(GAA;GAA)
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.179252186_179252188delGAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000184067.2,