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rs863223526

From SNPedia

Orientationplus
Make rs863223526(-;-)
Make rs863223526(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74046714
GeneELN
is asnp
is mentioned by
dbSNPrs863223526
ebirs863223526
HLIrs863223526
Exacrs863223526
Varsomers863223526
Maprs863223526
PheGenIrs863223526
hapmaprs863223526
1000 genomesrs863223526
hgdprs863223526
ensemblrs863223526
gopubmedrs863223526
geneviewrs863223526
scholarrs863223526
googlers863223526
pharmgkbrs863223526
gwascentralrs863223526
openSNPrs863223526
23andMers863223526
23andMe allrs863223526
SNP Nexus

SNPshotrs863223526
SNPdbers863223526
MSV3drs863223526
GWAS Ctlgrs863223526
Max Magnitude
ClinVar
Risk rs863223526(;)
Alt rs863223526(;)
Reference rs863223526(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73461044delG
CLNSRC
CLNACC RCV000196580.1,