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rs869025565

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025565(-;-)
Make rs869025565(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position150510997
GeneECM1, LOC105371435
is asnp
is mentioned by
dbSNPrs869025565
ebirs869025565
HLIrs869025565
Exacrs869025565
Varsomers869025565
Maprs869025565
PheGenIrs869025565
hapmaprs869025565
1000 genomesrs869025565
hgdprs869025565
ensemblrs869025565
gopubmedrs869025565
geneviewrs869025565
scholarrs869025565
googlers869025565
pharmgkbrs869025565
gwascentralrs869025565
openSNPrs869025565
23andMers869025565
23andMe allrs869025565
SNP Nexus

SNPshotrs869025565
SNPdbers869025565
MSV3drs869025565
GWAS Ctlgrs869025565
Max Magnitude0
ClinVar
Risk rs869025565(;)
Alt rs869025565(;)
Reference rs869025565(T;T)
Significance Pathogenic
Disease Lipid proteinosis
Variation info
Gene ECM1
CLNDBN Lipid proteinosis
Reversed 0
HGVS NC_000001.10:g.150483473delT
CLNSRC
CLNACC RCV000208549.1,