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rs1060500271

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500271(-;-)
Make rs1060500271(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31233072
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500271
dbSNP (old)rs1060500271
ClinGenrs1060500271
ebirs1060500271
HLIrs1060500271
Exacrs1060500271
Gnomadrs1060500271
Varsomers1060500271
LitVarrs1060500271
Maprs1060500271
PheGenIrs1060500271
Biobankrs1060500271
1000 genomesrs1060500271
hgdprs1060500271
ensemblrs1060500271
gopubmedrs1060500271
geneviewrs1060500271
scholarrs1060500271
googlers1060500271
pharmgkbrs1060500271
gwascentralrs1060500271
openSNPrs1060500271
23andMers1060500271
23andMe allrs1060500271
SNPshotrs1060500271
SNPdbers1060500271
MSV3drs1060500271
GWAS Ctlgrs1060500271
Max Magnitude0
ClinVar
Risk rs1060500271(-;-)
Alt rs1060500271(-;-)
Reference Rs1060500271(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29560090delA
CLNSRC
CLNACC RCV000463605.1,