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rs746217361

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746217361(C;T)
Make rs746217361(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position150511475
GeneECM1, LOC105371435
is asnp
is mentioned by
dbSNPrs746217361
ebirs746217361
HLIrs746217361
Exacrs746217361
Varsomers746217361
Maprs746217361
PheGenIrs746217361
hapmaprs746217361
1000 genomesrs746217361
hgdprs746217361
ensemblrs746217361
gopubmedrs746217361
geneviewrs746217361
scholarrs746217361
googlers746217361
pharmgkbrs746217361
gwascentralrs746217361
openSNPrs746217361
23andMers746217361
23andMe allrs746217361
SNP Nexus

SNPshotrs746217361
SNPdbers746217361
MSV3drs746217361
GWAS Ctlgrs746217361
Max Magnitude0
ClinVar
Risk rs746217361(A,T;A,T)
Alt rs746217361(A,T;A,T)
Reference rs746217361(C;C)
Significance Pathogenic
Disease Lipid proteinosis
Variation info
Gene ECM1
CLNDBN Lipid proteinosis
Reversed 0
HGVS NC_000001.10:g.150483951C>T
CLNSRC
CLNACC RCV000208570.1,