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rs62636503

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 6.1 Charcot-Marie-Tooth Disease, type 1
(G;G) 0 common in clinvar


Make rs62636503(A;A)
ReferenceGRCh38.p7 38.3/149
Chromosome8
Position24953779
GeneMIR6841, NEFL
is asnp
is mentioned by
dbSNPrs62636503
dbSNP (classic)rs62636503
ClinGenrs62636503
ebirs62636503
HLIrs62636503
Exacrs62636503
Gnomadrs62636503
Varsomers62636503
LitVarrs62636503
Maprs62636503
PheGenIrs62636503
Biobankrs62636503
1000 genomesrs62636503
hgdprs62636503
ensemblrs62636503
geneviewrs62636503
scholarrs62636503
googlers62636503
pharmgkbrs62636503
gwascentralrs62636503
openSNPrs62636503
23andMers62636503
SNPshotrs62636503
SNPdbers62636503
MSV3drs62636503
GWAS Ctlgrs62636503
Max Magnitude6.1
ClinVar
Risk rs62636503(A;A)
Alt rs62636503(A;A)
Reference Rs62636503(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR6841 NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24811293C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000057113.2,