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rs863223520

From SNPedia

Orientationplus
Make rs863223520(-;-)
Make rs863223520(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74054720
GeneELN
is asnp
is mentioned by
dbSNPrs863223520
ebirs863223520
HLIrs863223520
Exacrs863223520
Varsomers863223520
Maprs863223520
PheGenIrs863223520
hapmaprs863223520
1000 genomesrs863223520
hgdprs863223520
ensemblrs863223520
gopubmedrs863223520
geneviewrs863223520
scholarrs863223520
googlers863223520
pharmgkbrs863223520
gwascentralrs863223520
openSNPrs863223520
23andMers863223520
23andMe allrs863223520
SNP Nexus

SNPshotrs863223520
SNPdbers863223520
MSV3drs863223520
GWAS Ctlgrs863223520
Max Magnitude
ClinVar
Risk rs863223520(;)
Alt rs863223520(;)
Reference rs863223520(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73469050delT
CLNSRC
CLNACC RCV000195493.1,