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rs1051338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1051338(A;C)
Make rs1051338(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position89247603
GeneLIPA
is asnp
is mentioned by
dbSNPrs1051338
dbSNP (classic)rs1051338
ClinGenrs1051338
ebirs1051338
HLIrs1051338
Exacrs1051338
Gnomadrs1051338
Varsomers1051338
LitVarrs1051338
Maprs1051338
PheGenIrs1051338
Biobankrs1051338
1000 genomesrs1051338
hgdprs1051338
ensemblrs1051338
geneviewrs1051338
scholarrs1051338
googlers1051338
pharmgkbrs1051338
gwascentralrs1051338
openSNPrs1051338
23andMers1051338
SNPshotrs1051338
SNPdbers1051338
MSV3drs1051338
GWAS Ctlgrs1051338
GMAF0.275
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 22395809] Association of LIPA gene polymorphisms with obesity-related metabolic complications among severely obese patients


[PMID 16385451OA-icon.png] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.


[PMID 16730122] Influence of lysosomal acid lipase polymorphisms on chromosome 10 on the risk of Alzheimer's disease and cholesterol metabolism.



[PMID 288279971] Coronary Artery Disease-Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes.


ClinVar
Risk rs1051338(C;C)
Alt rs1051338(C;C)
Reference Rs1051338(A;A)
Significance Non-pathogenic
Disease not specified Wolman disease
Variation info
Gene LIPA
CLNDBN not specified Wolman disease
Reversed 1
HGVS NC_000010.10:g.91007360T>G
CLNSRC UniProtKB (protein)
CLNACC RCV000175562.2, RCV000350905.1,