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rs104893941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893941(C;T)
Make rs104893941(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position179836445
GeneSQSTM1
is asnp
is mentioned by
dbSNPrs104893941
ebirs104893941
HLIrs104893941
Exacrs104893941
Varsomers104893941
Maprs104893941
PheGenIrs104893941
hapmaprs104893941
1000 genomesrs104893941
hgdprs104893941
ensemblrs104893941
gopubmedrs104893941
geneviewrs104893941
scholarrs104893941
googlers104893941
pharmgkbrs104893941
gwascentralrs104893941
openSNPrs104893941
23andMers104893941
23andMe allrs104893941
SNP Nexus

SNPshotrs104893941
SNPdbers104893941
MSV3drs104893941
GWAS Ctlgrs104893941
GMAF0.004591
Max Magnitude0
OMIM601530
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893941(T;T)
Alt rs104893941(T;T)
Reference rs104893941(C;C)
Significance Other
Disease Paget disease of bone Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Variation info
Gene C5orf45 SQSTM1
CLNDBN Paget disease of bone, familial Frontotemporal dementia and/or amyotrophic lateral sclerosis 3
Reversed 0
HGVS NC_000005.9:g.179263445C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008576.4, RCV000184063.2,