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rs863223512

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223512(A;A)
Make rs863223512(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74043117
GeneELN
is asnp
is mentioned by
dbSNPrs863223512
ebirs863223512
HLIrs863223512
Exacrs863223512
Varsomers863223512
Maprs863223512
PheGenIrs863223512
hapmaprs863223512
1000 genomesrs863223512
hgdprs863223512
ensemblrs863223512
gopubmedrs863223512
geneviewrs863223512
scholarrs863223512
googlers863223512
pharmgkbrs863223512
gwascentralrs863223512
openSNPrs863223512
23andMers863223512
23andMe allrs863223512
SNP Nexus

SNPshotrs863223512
SNPdbers863223512
MSV3drs863223512
GWAS Ctlgrs863223512
Max Magnitude0
ClinVar
Risk rs863223512(A;A)
Alt rs863223512(A;A)
Reference rs863223512(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73457447G>A
CLNSRC
CLNACC RCV000199726.1,