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rs121909397

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909397(C;G)
Make rs121909397(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position869982
GeneLMF1
is asnp
is mentioned by
dbSNPrs121909397
ebirs121909397
HLIrs121909397
Exacrs121909397
Varsomers121909397
Maprs121909397
PheGenIrs121909397
hapmaprs121909397
1000 genomesrs121909397
hgdprs121909397
ensemblrs121909397
gopubmedrs121909397
geneviewrs121909397
scholarrs121909397
googlers121909397
pharmgkbrs121909397
gwascentralrs121909397
openSNPrs121909397
23andMers121909397
23andMe allrs121909397
SNP Nexus

SNPshotrs121909397
SNPdbers121909397
MSV3drs121909397
GWAS Ctlgrs121909397
Max Magnitude0
OMIM611761
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909397(T;T)
Alt rs121909397(T;T)
Reference rs121909397(C;C)
Significance Pathogenic
Disease Lipase deficiency combined
Variation info
Gene LMF1
CLNDBN Lipase deficiency combined
Reversed 1
HGVS NC_000016.9:g.919982G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000828.2,