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rs863223517

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223517(A;A)
Make rs863223517(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74063374
GeneELN
is asnp
is mentioned by
dbSNPrs863223517
ebirs863223517
HLIrs863223517
Exacrs863223517
Varsomers863223517
Maprs863223517
PheGenIrs863223517
hapmaprs863223517
1000 genomesrs863223517
hgdprs863223517
ensemblrs863223517
gopubmedrs863223517
geneviewrs863223517
scholarrs863223517
googlers863223517
pharmgkbrs863223517
gwascentralrs863223517
openSNPrs863223517
23andMers863223517
23andMe allrs863223517
SNP Nexus

SNPshotrs863223517
SNPdbers863223517
MSV3drs863223517
GWAS Ctlgrs863223517
Max Magnitude0
ClinVar
Risk rs863223517(A;A)
Alt rs863223517(A;A)
Reference rs863223517(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73477704G>A
CLNSRC
CLNACC RCV000200555.1,