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rs863223521

From SNPedia

Orientationplus
Make rs863223521(-;-)
Make rs863223521(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74056281
GeneELN
is asnp
is mentioned by
dbSNPrs863223521
ebirs863223521
HLIrs863223521
Exacrs863223521
Varsomers863223521
Maprs863223521
PheGenIrs863223521
hapmaprs863223521
1000 genomesrs863223521
hgdprs863223521
ensemblrs863223521
gopubmedrs863223521
geneviewrs863223521
scholarrs863223521
googlers863223521
pharmgkbrs863223521
gwascentralrs863223521
openSNPrs863223521
23andMers863223521
23andMe allrs863223521
SNP Nexus

SNPshotrs863223521
SNPdbers863223521
MSV3drs863223521
GWAS Ctlgrs863223521
Max Magnitude
ClinVar
Risk rs863223521(;)
Alt rs863223521(;)
Reference rs863223521(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73470611delC
CLNSRC
CLNACC RCV000197682.1,