Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223513

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223513(A;A)
Make rs863223513(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74046742
GeneELN
is asnp
is mentioned by
dbSNPrs863223513
ebirs863223513
HLIrs863223513
Exacrs863223513
Varsomers863223513
Maprs863223513
PheGenIrs863223513
hapmaprs863223513
1000 genomesrs863223513
hgdprs863223513
ensemblrs863223513
gopubmedrs863223513
geneviewrs863223513
scholarrs863223513
googlers863223513
pharmgkbrs863223513
gwascentralrs863223513
openSNPrs863223513
23andMers863223513
23andMe allrs863223513
SNP Nexus

SNPshotrs863223513
SNPdbers863223513
MSV3drs863223513
GWAS Ctlgrs863223513
Max Magnitude0
ClinVar
Risk rs863223513(A;A)
Alt rs863223513(A;A)
Reference rs863223513(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73461072T>A
CLNSRC
CLNACC RCV000196516.2,