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rs863223511

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223511(A;C)
Make rs863223511(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74043116
GeneELN
is asnp
is mentioned by
dbSNPrs863223511
ebirs863223511
HLIrs863223511
Exacrs863223511
Varsomers863223511
Maprs863223511
PheGenIrs863223511
hapmaprs863223511
1000 genomesrs863223511
hgdprs863223511
ensemblrs863223511
gopubmedrs863223511
geneviewrs863223511
scholarrs863223511
googlers863223511
pharmgkbrs863223511
gwascentralrs863223511
openSNPrs863223511
23andMers863223511
23andMe allrs863223511
SNP Nexus

SNPshotrs863223511
SNPdbers863223511
MSV3drs863223511
GWAS Ctlgrs863223511
Max Magnitude0
ClinVar
Risk rs863223511(C;C)
Alt rs863223511(C;C)
Reference rs863223511(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73457446A>C
CLNSRC
CLNACC RCV000197464.1,