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

rs587777626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777626(C;T)
Make rs587777626(T;T)
ReferenceGRCh38 38.1/142
Chromosome16
Position869908
GeneLMF1
is asnp
is mentioned by
dbSNPrs587777626
ebirs587777626
HLIrs587777626
Exacrs587777626
Varsomers587777626
Maprs587777626
PheGenIrs587777626
hapmaprs587777626
1000 genomesrs587777626
hgdprs587777626
ensemblrs587777626
gopubmedrs587777626
geneviewrs587777626
scholarrs587777626
googlers587777626
pharmgkbrs587777626
gwascentralrs587777626
openSNPrs587777626
23andMers587777626
23andMe allrs587777626
SNP Nexus

SNPshotrs587777626
SNPdbers587777626
MSV3drs587777626
GWAS Ctlgrs587777626
Max Magnitude0
ClinVar
Risk rs587777626(C,T;C,T)
Alt rs587777626(C,T;C,T)
Reference rs587777626(G;G)
Significance Pathogenic
Disease Lipase deficiency combined
Variation info
Gene LMF1
CLNDBN Lipase deficiency combined
Reversed 1
HGVS NC_000016.9:g.919908C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133508.3,