Have questions? Visit https://www.reddit.com/r/SNPedia

rs116928232

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs116928232(C;T)
Make rs116928232(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position89222511
GeneLIPA
is asnp
is mentioned by
dbSNPrs116928232
ebirs116928232
HLIrs116928232
Exacrs116928232
Varsomers116928232
Maprs116928232
PheGenIrs116928232
hapmaprs116928232
1000 genomesrs116928232
hgdprs116928232
ensemblrs116928232
gopubmedrs116928232
geneviewrs116928232
scholarrs116928232
googlers116928232
pharmgkbrs116928232
gwascentralrs116928232
openSNPrs116928232
23andMers116928232
23andMe allrs116928232
SNP Nexus

SNPshotrs116928232
SNPdbers116928232
MSV3drs116928232
GWAS Ctlgrs116928232
Max Magnitude0
ClinVar
Risk rs116928232(T;T)
Alt rs116928232(T;T)
Reference rs116928232(C;C)
Significance Pathogenic
Disease Lysosomal acid lipase deficiency
Variation info
Gene LIPA
CLNDBN Lysosomal acid lipase deficiency
Reversed 0
HGVS NC_000010.10:g.90982268C>T
CLNSRC
CLNACC RCV000185528.3,