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rs863223518

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223518(C;C)
Make rs863223518(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74028189
GeneELN
is asnp
is mentioned by
dbSNPrs863223518
ebirs863223518
HLIrs863223518
Exacrs863223518
Varsomers863223518
Maprs863223518
PheGenIrs863223518
hapmaprs863223518
1000 genomesrs863223518
hgdprs863223518
ensemblrs863223518
gopubmedrs863223518
geneviewrs863223518
scholarrs863223518
googlers863223518
pharmgkbrs863223518
gwascentralrs863223518
openSNPrs863223518
23andMers863223518
23andMe allrs863223518
SNP Nexus

SNPshotrs863223518
SNPdbers863223518
MSV3drs863223518
GWAS Ctlgrs863223518
Max Magnitude0
ClinVar
Risk rs863223518(C;C)
Alt rs863223518(C;C)
Reference rs863223518(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73442519T>C
CLNSRC
CLNACC RCV000195606.1,