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rs62636502

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs62636502(C;C)
Make rs62636502(C;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position24955713
GeneMIR6841, NEFL
is asnp
is mentioned by
dbSNPrs62636502
ebirs62636502
HLIrs62636502
Exacrs62636502
Varsomers62636502
Maprs62636502
PheGenIrs62636502
hapmaprs62636502
1000 genomesrs62636502
hgdprs62636502
ensemblrs62636502
gopubmedrs62636502
geneviewrs62636502
scholarrs62636502
googlers62636502
pharmgkbrs62636502
gwascentralrs62636502
openSNPrs62636502
23andMers62636502
23andMe allrs62636502
SNP Nexus

SNPshotrs62636502
SNPdbers62636502
MSV3drs62636502
GWAS Ctlgrs62636502
Max Magnitude0
ClinVar
Risk rs62636502(C,G;C,G)
Alt rs62636502(C,G;C,G)
Reference rs62636502(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6841 NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24813227A>C; NC_000008.10:g.24813227A>G
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000143811.1, RCV000057148.1,