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rs863223519

From SNPedia

Orientationplus
Make rs863223519(-;-)
Make rs863223519(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74045229
GeneELN
is asnp
is mentioned by
dbSNPrs863223519
ebirs863223519
HLIrs863223519
Exacrs863223519
Varsomers863223519
Maprs863223519
PheGenIrs863223519
hapmaprs863223519
1000 genomesrs863223519
hgdprs863223519
ensemblrs863223519
gopubmedrs863223519
geneviewrs863223519
scholarrs863223519
googlers863223519
pharmgkbrs863223519
gwascentralrs863223519
openSNPrs863223519
23andMers863223519
23andMe allrs863223519
SNP Nexus

SNPshotrs863223519
SNPdbers863223519
MSV3drs863223519
GWAS Ctlgrs863223519
Max Magnitude
ClinVar
Risk rs863223519(;)
Alt rs863223519(;)
Reference rs863223519(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73459559delG
CLNSRC
CLNACC RCV000197846.1,