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rs1060500385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500385(C;G)
Make rs1060500385(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31349244
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500385
dbSNP (old)rs1060500385
ClinGenrs1060500385
ebirs1060500385
HLIrs1060500385
Exacrs1060500385
Gnomadrs1060500385
Varsomers1060500385
Maprs1060500385
PheGenIrs1060500385
Biobankrs1060500385
1000 genomesrs1060500385
hgdprs1060500385
ensemblrs1060500385
gopubmedrs1060500385
geneviewrs1060500385
scholarrs1060500385
googlers1060500385
pharmgkbrs1060500385
gwascentralrs1060500385
openSNPrs1060500385
23andMers1060500385
23andMe allrs1060500385
SNPshotrs1060500385
SNPdbers1060500385
MSV3drs1060500385
GWAS Ctlgrs1060500385
Max Magnitude0
ClinVar
Risk rs1060500385(G;G)
Alt rs1060500385(G;G)
Reference Rs1060500385(C;C)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29676262C>G
CLNSRC
CLNACC RCV000472189.1,