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rs587777882

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777882(C;T)
Make rs587777882(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position24953646
GeneMIR6841, NEFL
is asnp
is mentioned by
dbSNPrs587777882
ebirs587777882
HLIrs587777882
Exacrs587777882
Varsomers587777882
Maprs587777882
PheGenIrs587777882
hapmaprs587777882
1000 genomesrs587777882
hgdprs587777882
ensemblrs587777882
gopubmedrs587777882
geneviewrs587777882
scholarrs587777882
googlers587777882
pharmgkbrs587777882
gwascentralrs587777882
openSNPrs587777882
23andMers587777882
23andMe allrs587777882
SNP Nexus

SNPshotrs587777882
SNPdbers587777882
MSV3drs587777882
GWAS Ctlgrs587777882
Max Magnitude0
ClinVar
Risk rs587777882(T;T)
Alt rs587777882(T;T)
Reference rs587777882(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6841 NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24811160G>A
CLNSRC
CLNACC RCV000143808.1,