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rs587778878

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778878(G;T)
Make rs587778878(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position89228368
GeneLIPA
is asnp
is mentioned by
dbSNPrs587778878
ebirs587778878
HLIrs587778878
Exacrs587778878
Varsomers587778878
Maprs587778878
PheGenIrs587778878
hapmaprs587778878
1000 genomesrs587778878
hgdprs587778878
ensemblrs587778878
gopubmedrs587778878
geneviewrs587778878
scholarrs587778878
googlers587778878
pharmgkbrs587778878
gwascentralrs587778878
openSNPrs587778878
23andMers587778878
23andMe allrs587778878
SNP Nexus

SNPshotrs587778878
SNPdbers587778878
MSV3drs587778878
GWAS Ctlgrs587778878
Max Magnitude0
ClinVar
Risk rs587778878(T;T)
Alt rs587778878(T;T)
Reference rs587778878(G;G)
Significance Pathogenic
Disease Lysosomal acid lipase deficiency
Variation info
Gene LIPA
CLNDBN Lysosomal acid lipase deficiency
Reversed 1
HGVS NC_000010.10:g.90988125C>A
CLNSRC
CLNACC RCV000191997.1,