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rs869025563

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025563(C;T)
Make rs869025563(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position150511574
GeneECM1, LOC105371435
is asnp
is mentioned by
dbSNPrs869025563
ClinGenrs869025563
ebirs869025563
HLIrs869025563
Exacrs869025563
Varsomers869025563
Maprs869025563
PheGenIrs869025563
hapmaprs869025563
1000 genomesrs869025563
hgdprs869025563
ensemblrs869025563
gopubmedrs869025563
geneviewrs869025563
scholarrs869025563
googlers869025563
pharmgkbrs869025563
gwascentralrs869025563
openSNPrs869025563
23andMers869025563
23andMe allrs869025563
SNP Nexus

SNPshotrs869025563
SNPdbers869025563
MSV3drs869025563
GWAS Ctlgrs869025563
Max Magnitude0
ClinVar
Risk rs869025563(T;T)
Alt rs869025563(T;T)
Reference Rs869025563(C;C)
Significance Pathogenic
Disease Lipid proteinosis
Variation info
Gene ECM1
CLNDBN Lipid proteinosis
Reversed 0
HGVS NC_000001.10:g.150484050C>T
CLNSRC
CLNACC RCV000208541.1,