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rs863223527

From SNPedia

Orientationplus
Make rs863223527(-;-)
Make rs863223527(-;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74048184
GeneELN
is asnp
is mentioned by
dbSNPrs863223527
ebirs863223527
HLIrs863223527
Exacrs863223527
Varsomers863223527
Maprs863223527
PheGenIrs863223527
hapmaprs863223527
1000 genomesrs863223527
hgdprs863223527
ensemblrs863223527
gopubmedrs863223527
geneviewrs863223527
scholarrs863223527
googlers863223527
pharmgkbrs863223527
gwascentralrs863223527
openSNPrs863223527
23andMers863223527
23andMe allrs863223527
SNP Nexus

SNPshotrs863223527
SNPdbers863223527
MSV3drs863223527
GWAS Ctlgrs863223527
Max Magnitude
ClinVar
Risk rs863223527(;)
Alt rs863223527(;)
Reference rs863223527(GT;GT)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73462514_73462515delGT
CLNSRC
CLNACC RCV000198657.1,