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rs863223516

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223516(A;A)
Make rs863223516(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74063309
GeneELN
is asnp
is mentioned by
dbSNPrs863223516
ebirs863223516
HLIrs863223516
Exacrs863223516
Varsomers863223516
Maprs863223516
PheGenIrs863223516
hapmaprs863223516
1000 genomesrs863223516
hgdprs863223516
ensemblrs863223516
gopubmedrs863223516
geneviewrs863223516
scholarrs863223516
googlers863223516
pharmgkbrs863223516
gwascentralrs863223516
openSNPrs863223516
23andMers863223516
23andMe allrs863223516
SNP Nexus

SNPshotrs863223516
SNPdbers863223516
MSV3drs863223516
GWAS Ctlgrs863223516
Max Magnitude0
ClinVar
Risk rs863223516(A;A)
Alt rs863223516(A;A)
Reference rs863223516(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73477639G>A
CLNSRC
CLNACC RCV000199115.1,