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rs1060500327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060500327(-;-)
Make rs1060500327(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31352406
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500327
dbSNP (old)rs1060500327
ClinGenrs1060500327
ebirs1060500327
HLIrs1060500327
Exacrs1060500327
Gnomadrs1060500327
Varsomers1060500327
LitVarrs1060500327
Maprs1060500327
PheGenIrs1060500327
Biobankrs1060500327
1000 genomesrs1060500327
hgdprs1060500327
ensemblrs1060500327
gopubmedrs1060500327
geneviewrs1060500327
scholarrs1060500327
googlers1060500327
pharmgkbrs1060500327
gwascentralrs1060500327
openSNPrs1060500327
23andMers1060500327
23andMe allrs1060500327
SNPshotrs1060500327
SNPdbers1060500327
MSV3drs1060500327
GWAS Ctlgrs1060500327
Max Magnitude0
ClinVar
Risk rs1060500327(-;-)
Alt rs1060500327(-;-)
Reference Rs1060500327(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29679424delA
CLNSRC
CLNACC RCV000466333.1,