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rs1057517776

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517776(G;G)
Make rs1057517776(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position24956222
GeneNEFL
is asnp
is mentioned by
dbSNPrs1057517776
dbSNP (old)rs1057517776
ClinGenrs1057517776
ebirs1057517776
HLIrs1057517776
Exacrs1057517776
Gnomadrs1057517776
Varsomers1057517776
LitVarrs1057517776
Maprs1057517776
PheGenIrs1057517776
Biobankrs1057517776
1000 genomesrs1057517776
hgdprs1057517776
ensemblrs1057517776
gopubmedrs1057517776
geneviewrs1057517776
scholarrs1057517776
googlers1057517776
pharmgkbrs1057517776
gwascentralrs1057517776
openSNPrs1057517776
23andMers1057517776
23andMe allrs1057517776
SNPshotrs1057517776
SNPdbers1057517776
MSV3drs1057517776
GWAS Ctlgrs1057517776
Max Magnitude0
ClinVar
Risk rs1057517776(G;G)
Alt rs1057517776(G;G)
Reference Rs1057517776(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEFL
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.24813736A>C
CLNSRC
CLNACC RCV000413716.1,