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rs863223522

From SNPedia

Orientationplus
Make rs863223522(-;-)
Make rs863223522(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74056315
GeneELN
is asnp
is mentioned by
dbSNPrs863223522
ebirs863223522
HLIrs863223522
Exacrs863223522
Varsomers863223522
Maprs863223522
PheGenIrs863223522
hapmaprs863223522
1000 genomesrs863223522
hgdprs863223522
ensemblrs863223522
gopubmedrs863223522
geneviewrs863223522
scholarrs863223522
googlers863223522
pharmgkbrs863223522
gwascentralrs863223522
openSNPrs863223522
23andMers863223522
23andMe allrs863223522
SNP Nexus

SNPshotrs863223522
SNPdbers863223522
MSV3drs863223522
GWAS Ctlgrs863223522
Max Magnitude
ClinVar
Risk rs863223522(;)
Alt rs863223522(;)
Reference rs863223522(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73470645delG
CLNSRC
CLNACC RCV000200111.1,