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rs1060500358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500358(A;G)
Make rs1060500358(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31201035
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500358
dbSNP (old)rs1060500358
ClinGenrs1060500358
ebirs1060500358
HLIrs1060500358
Exacrs1060500358
Gnomadrs1060500358
Varsomers1060500358
LitVarrs1060500358
Maprs1060500358
PheGenIrs1060500358
Biobankrs1060500358
1000 genomesrs1060500358
hgdprs1060500358
ensemblrs1060500358
gopubmedrs1060500358
geneviewrs1060500358
scholarrs1060500358
googlers1060500358
pharmgkbrs1060500358
gwascentralrs1060500358
openSNPrs1060500358
23andMers1060500358
23andMe allrs1060500358
SNPshotrs1060500358
SNPdbers1060500358
MSV3drs1060500358
GWAS Ctlgrs1060500358
Max Magnitude0
ClinVar
Risk rs1060500358(G;G)
Alt rs1060500358(G;G)
Reference Rs1060500358(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29528053A>G
CLNSRC
CLNACC RCV000471389.1,