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rs878854452

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854452(-;-)
Make rs878854452(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position74043158
GeneELN
is asnp
is mentioned by
dbSNPrs878854452
ebirs878854452
HLIrs878854452
Exacrs878854452
Varsomers878854452
Maprs878854452
PheGenIrs878854452
hapmaprs878854452
1000 genomesrs878854452
hgdprs878854452
ensemblrs878854452
gopubmedrs878854452
geneviewrs878854452
scholarrs878854452
googlers878854452
pharmgkbrs878854452
gwascentralrs878854452
openSNPrs878854452
23andMers878854452
23andMe allrs878854452
SNP Nexus

SNPshotrs878854452
SNPdbers878854452
MSV3drs878854452
GWAS Ctlgrs878854452
Max Magnitude0
ClinVar
Risk rs878854452(;)
Alt rs878854452(;)
Reference rs878854452(G;G)
Significance Pathogenic
Disease Supravalvar aortic stenosis
Variation info
Gene ELN
CLNDBN Supravalvar aortic stenosis
Reversed 0
HGVS NC_000007.13:g.73457488delG
CLNSRC
CLNACC RCV000232952.1,