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rs1060500333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060500333(G;G)
Make rs1060500333(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31357319
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500333
dbSNP (old)rs1060500333
ClinGenrs1060500333
ebirs1060500333
HLIrs1060500333
Exacrs1060500333
Gnomadrs1060500333
Varsomers1060500333
LitVarrs1060500333
Maprs1060500333
PheGenIrs1060500333
Biobankrs1060500333
1000 genomesrs1060500333
hgdprs1060500333
ensemblrs1060500333
gopubmedrs1060500333
geneviewrs1060500333
scholarrs1060500333
googlers1060500333
pharmgkbrs1060500333
gwascentralrs1060500333
openSNPrs1060500333
23andMers1060500333
23andMe allrs1060500333
SNPshotrs1060500333
SNPdbers1060500333
MSV3drs1060500333
GWAS Ctlgrs1060500333
Max Magnitude0
ClinVar
Risk rs1060500333(G;G)
Alt rs1060500333(G;G)
Reference Rs1060500333(T;T)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29684337T>G
CLNSRC
CLNACC RCV000456882.1,