Have questions? Visit https://www.reddit.com/r/SNPedia

rs782755390

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs782755390(C;T)
Make rs782755390(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74068650
GeneELN
is asnp
is mentioned by
dbSNPrs782755390
ebirs782755390
HLIrs782755390
Exacrs782755390
Varsomers782755390
Maprs782755390
PheGenIrs782755390
hapmaprs782755390
1000 genomesrs782755390
hgdprs782755390
ensemblrs782755390
gopubmedrs782755390
geneviewrs782755390
scholarrs782755390
googlers782755390
pharmgkbrs782755390
gwascentralrs782755390
openSNPrs782755390
23andMers782755390
23andMe allrs782755390
SNP Nexus

SNPshotrs782755390
SNPdbers782755390
MSV3drs782755390
GWAS Ctlgrs782755390
Max Magnitude0
ClinVar
Risk rs782755390(T;T)
Alt rs782755390(T;T)
Reference rs782755390(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELN
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.73482980C>A
CLNSRC
CLNACC RCV000198856.1,