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rs1060500255

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500255(A;A)
Make rs1060500255(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31325997
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500255
dbSNP (classic)rs1060500255
ClinGenrs1060500255
ebirs1060500255
HLIrs1060500255
Exacrs1060500255
Gnomadrs1060500255
Varsomers1060500255
LitVarrs1060500255
Maprs1060500255
PheGenIrs1060500255
Biobankrs1060500255
1000 genomesrs1060500255
hgdprs1060500255
ensemblrs1060500255
geneviewrs1060500255
scholarrs1060500255
googlers1060500255
pharmgkbrs1060500255
gwascentralrs1060500255
openSNPrs1060500255
23andMers1060500255
23andMe allrs1060500255
SNPshotrs1060500255
SNPdbers1060500255
MSV3drs1060500255
GWAS Ctlgrs1060500255
Max Magnitude0
ClinVar
Risk rs1060500255(A;A)
Alt rs1060500255(A;A)
Reference Rs1060500255(C;C)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29653015C>A
CLNSRC
CLNACC RCV000458556.1,