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rs121912502

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912502(C;T)
Make rs121912502(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position58548387
GeneLIPC
is asnp
is mentioned by
dbSNPrs121912502
ebirs121912502
HLIrs121912502
Exacrs121912502
Varsomers121912502
Maprs121912502
PheGenIrs121912502
hapmaprs121912502
1000 genomesrs121912502
hgdprs121912502
ensemblrs121912502
gopubmedrs121912502
geneviewrs121912502
scholarrs121912502
googlers121912502
pharmgkbrs121912502
gwascentralrs121912502
openSNPrs121912502
23andMers121912502
23andMe allrs121912502
SNP Nexus

SNPshotrs121912502
SNPdbers121912502
MSV3drs121912502
GWAS Ctlgrs121912502
GMAF0.0004591
Max Magnitude0
OMIM151670
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912502(T;T)
Alt rs121912502(T;T)
Reference rs121912502(C;C)
Significance Other
Disease Hepatic lipase deficiency
Variation info
Gene LIPC
CLNDBN Hepatic lipase deficiency
Reversed 0
HGVS NC_000015.9:g.58840586C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015537.25,