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rs587777880

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777880(A;G)
Make rs587777880(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position24955722
GeneMIR6841, NEFL
is asnp
is mentioned by
dbSNPrs587777880
ebirs587777880
HLIrs587777880
Exacrs587777880
Varsomers587777880
Maprs587777880
PheGenIrs587777880
hapmaprs587777880
1000 genomesrs587777880
hgdprs587777880
ensemblrs587777880
gopubmedrs587777880
geneviewrs587777880
scholarrs587777880
googlers587777880
pharmgkbrs587777880
gwascentralrs587777880
openSNPrs587777880
23andMers587777880
23andMe allrs587777880
SNP Nexus

SNPshotrs587777880
SNPdbers587777880
MSV3drs587777880
GWAS Ctlgrs587777880
Max Magnitude0
ClinVar
Risk rs587777880(G;G)
Alt rs587777880(G;G)
Reference rs587777880(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6841 NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24813236T>C
CLNSRC
CLNACC RCV000143810.1,