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rs58982919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs58982919(A;G)
Make rs58982919(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position24956223
GeneNEFL
is asnp
is mentioned by
dbSNPrs58982919
ebirs58982919
HLIrs58982919
Exacrs58982919
Varsomers58982919
Maprs58982919
PheGenIrs58982919
hapmaprs58982919
1000 genomesrs58982919
hgdprs58982919
ensemblrs58982919
gopubmedrs58982919
geneviewrs58982919
scholarrs58982919
googlers58982919
pharmgkbrs58982919
gwascentralrs58982919
openSNPrs58982919
23andMers58982919
23andMe allrs58982919
SNP Nexus

SNPshotrs58982919
SNPdbers58982919
MSV3drs58982919
GWAS Ctlgrs58982919
Max Magnitude0
ClinVar
Risk rs58982919(G;G)
Alt rs58982919(G;G)
Reference rs58982919(A;A)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease not provided
Variation info
Gene NEFL
CLNDBN Charcot-Marie-Tooth disease, demyelinating, type 1f not provided
Reversed 1
HGVS NC_000008.10:g.24813737T>C
CLNSRC ClinVar Epithelial Biology GeneReviews
CLNACC RCV000034136.2, RCV000057136.2,