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rs863223515

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223515(G;T)
Make rs863223515(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74063176
GeneELN
is asnp
is mentioned by
dbSNPrs863223515
ebirs863223515
HLIrs863223515
Exacrs863223515
Varsomers863223515
Maprs863223515
PheGenIrs863223515
hapmaprs863223515
1000 genomesrs863223515
hgdprs863223515
ensemblrs863223515
gopubmedrs863223515
geneviewrs863223515
scholarrs863223515
googlers863223515
pharmgkbrs863223515
gwascentralrs863223515
openSNPrs863223515
23andMers863223515
23andMe allrs863223515
SNP Nexus

SNPshotrs863223515
SNPdbers863223515
MSV3drs863223515
GWAS Ctlgrs863223515
Max Magnitude0
ClinVar
Risk rs863223515(T;T)
Alt rs863223515(T;T)
Reference rs863223515(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73477506G>T
CLNSRC
CLNACC RCV000196900.1,