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rs587777881

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777881(C;C)
Make rs587777881(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position24955509
GeneMIR6841, NEFL
is asnp
is mentioned by
dbSNPrs587777881
ebirs587777881
HLIrs587777881
Exacrs587777881
Varsomers587777881
Maprs587777881
PheGenIrs587777881
hapmaprs587777881
1000 genomesrs587777881
hgdprs587777881
ensemblrs587777881
gopubmedrs587777881
geneviewrs587777881
scholarrs587777881
googlers587777881
pharmgkbrs587777881
gwascentralrs587777881
openSNPrs587777881
23andMers587777881
23andMe allrs587777881
SNP Nexus

SNPshotrs587777881
SNPdbers587777881
MSV3drs587777881
GWAS Ctlgrs587777881
Max Magnitude0
ClinVar
Risk rs587777881(C;C)
Alt rs587777881(C;C)
Reference rs587777881(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6841 NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24813023A>G
CLNSRC
CLNACC RCV000143807.1,