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rs201012726

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201012726(C;T)
Make rs201012726(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74047690
GeneELN
is asnp
is mentioned by
dbSNPrs201012726
ebirs201012726
HLIrs201012726
Exacrs201012726
Varsomers201012726
Maprs201012726
PheGenIrs201012726
hapmaprs201012726
1000 genomesrs201012726
hgdprs201012726
ensemblrs201012726
gopubmedrs201012726
geneviewrs201012726
scholarrs201012726
googlers201012726
pharmgkbrs201012726
gwascentralrs201012726
openSNPrs201012726
23andMers201012726
23andMe allrs201012726
SNP Nexus

SNPshotrs201012726
SNPdbers201012726
MSV3drs201012726
GWAS Ctlgrs201012726
Max Magnitude0
ClinVar
Risk rs201012726(T;T)
Alt rs201012726(T;T)
Reference rs201012726(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73462020C>T
CLNSRC
CLNACC RCV000198008.2,