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rs869025566

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025566(G;G)
Make rs869025566(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position150511148
GeneECM1, LOC105371435
is asnp
is mentioned by
dbSNPrs869025566
ebirs869025566
HLIrs869025566
Exacrs869025566
Varsomers869025566
Maprs869025566
PheGenIrs869025566
hapmaprs869025566
1000 genomesrs869025566
hgdprs869025566
ensemblrs869025566
gopubmedrs869025566
geneviewrs869025566
scholarrs869025566
googlers869025566
pharmgkbrs869025566
gwascentralrs869025566
openSNPrs869025566
23andMers869025566
23andMe allrs869025566
SNP Nexus

SNPshotrs869025566
SNPdbers869025566
MSV3drs869025566
GWAS Ctlgrs869025566
Max Magnitude0
ClinVar
Risk rs869025566(G;G)
Alt rs869025566(G;G)
Reference rs869025566(T;T)
Significance Pathogenic
Disease Lipid proteinosis
Variation info
Gene ECM1
CLNDBN Lipid proteinosis
Reversed 0
HGVS NC_000001.10:g.150483624T>G
CLNSRC
CLNACC RCV000208554.1,