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rs121909115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909115(C;T)
Make rs121909115(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position150509696
GeneECM1
is asnp
is mentioned by
dbSNPrs121909115
ebirs121909115
HLIrs121909115
Exacrs121909115
Varsomers121909115
Maprs121909115
PheGenIrs121909115
hapmaprs121909115
1000 genomesrs121909115
hgdprs121909115
ensemblrs121909115
gopubmedrs121909115
geneviewrs121909115
scholarrs121909115
googlers121909115
pharmgkbrs121909115
gwascentralrs121909115
openSNPrs121909115
23andMers121909115
23andMe allrs121909115
SNP Nexus

SNPshotrs121909115
SNPdbers121909115
MSV3drs121909115
GWAS Ctlgrs121909115
Max Magnitude0
OMIM602201
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909115(T;T)
Alt rs121909115(T;T)
Reference rs121909115(C;C)
Significance Pathogenic
Disease Lipid proteinosis
Variation info
Gene ECM1
CLNDBN Lipid proteinosis
Reversed 0
HGVS NC_000001.10:g.150482172C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007901.2,