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rs863223514

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223514(G;T)
Make rs863223514(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74061106
GeneELN
is asnp
is mentioned by
dbSNPrs863223514
ebirs863223514
HLIrs863223514
Exacrs863223514
Varsomers863223514
Maprs863223514
PheGenIrs863223514
hapmaprs863223514
1000 genomesrs863223514
hgdprs863223514
ensemblrs863223514
gopubmedrs863223514
geneviewrs863223514
scholarrs863223514
googlers863223514
pharmgkbrs863223514
gwascentralrs863223514
openSNPrs863223514
23andMers863223514
23andMe allrs863223514
SNP Nexus

SNPshotrs863223514
SNPdbers863223514
MSV3drs863223514
GWAS Ctlgrs863223514
Max Magnitude0
ClinVar
Risk rs863223514(T;T)
Alt rs863223514(T;T)
Reference rs863223514(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73475436G>T
CLNSRC
CLNACC RCV000200864.1,