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rs1057518134

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518134(C;T)
Make rs1057518134(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31219068
GeneNF1
is asnp
is mentioned by
dbSNPrs1057518134
dbSNP (old)rs1057518134
ClinGenrs1057518134
ebirs1057518134
HLIrs1057518134
Exacrs1057518134
Gnomadrs1057518134
Varsomers1057518134
LitVarrs1057518134
Maprs1057518134
PheGenIrs1057518134
Biobankrs1057518134
1000 genomesrs1057518134
hgdprs1057518134
ensemblrs1057518134
gopubmedrs1057518134
geneviewrs1057518134
scholarrs1057518134
googlers1057518134
pharmgkbrs1057518134
gwascentralrs1057518134
openSNPrs1057518134
23andMers1057518134
23andMe allrs1057518134
SNPshotrs1057518134
SNPdbers1057518134
MSV3drs1057518134
GWAS Ctlgrs1057518134
Max Magnitude0
ClinVar
Risk rs1057518134(T;T)
Alt rs1057518134(T;T)
Reference Rs1057518134(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29546086C>T
CLNSRC
CLNACC RCV000413398.1,