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rs1064793880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position74046755
GeneELN
is asnp
is mentioned by
dbSNPrs1064793880
dbSNP (old)rs1064793880
ClinGenrs1064793880
ebirs1064793880
HLIrs1064793880
Exacrs1064793880
Gnomadrs1064793880
Varsomers1064793880
LitVarrs1064793880
Maprs1064793880
PheGenIrs1064793880
Biobankrs1064793880
1000 genomesrs1064793880
hgdprs1064793880
ensemblrs1064793880
gopubmedrs1064793880
geneviewrs1064793880
scholarrs1064793880
googlers1064793880
pharmgkbrs1064793880
gwascentralrs1064793880
openSNPrs1064793880
23andMers1064793880
23andMe allrs1064793880
SNPshotrs1064793880
SNPdbers1064793880
MSV3drs1064793880
GWAS Ctlgrs1064793880
Max Magnitude0
ClinVar
Risk rs1064793880(T;T)
Alt rs1064793880(T;T)
Reference Rs1064793880(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73461085C>T
CLNSRC
CLNACC RCV000486139.1,