Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223528

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223528(-;C)
Make rs863223528(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74051798
GeneELN
is asnp
is mentioned by
dbSNPrs863223528
ClinGenrs863223528
ebirs863223528
HLIrs863223528
Exacrs863223528
Varsomers863223528
Maprs863223528
PheGenIrs863223528
hapmaprs863223528
1000 genomesrs863223528
hgdprs863223528
ensemblrs863223528
gopubmedrs863223528
geneviewrs863223528
scholarrs863223528
googlers863223528
pharmgkbrs863223528
gwascentralrs863223528
openSNPrs863223528
23andMers863223528
23andMe allrs863223528
SNP Nexus

SNPshotrs863223528
SNPdbers863223528
MSV3drs863223528
GWAS Ctlgrs863223528
Max Magnitude0
ClinVar
Risk rs863223528(C;C)
Alt rs863223528(C;C)
Reference Rs863223528(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73466128dupC
CLNSRC
CLNACC RCV000200220.1,