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rs1060500387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1060500387(-;-)
Make rs1060500387(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position31358568
GeneNF1
is asnp
is mentioned by
dbSNPrs1060500387
dbSNP (classic)rs1060500387
ClinGenrs1060500387
ebirs1060500387
HLIrs1060500387
Exacrs1060500387
Gnomadrs1060500387
Varsomers1060500387
LitVarrs1060500387
Maprs1060500387
PheGenIrs1060500387
Biobankrs1060500387
1000 genomesrs1060500387
hgdprs1060500387
ensemblrs1060500387
geneviewrs1060500387
scholarrs1060500387
googlers1060500387
pharmgkbrs1060500387
gwascentralrs1060500387
openSNPrs1060500387
23andMers1060500387
23andMe allrs1060500387
SNPshotrs1060500387
SNPdbers1060500387
MSV3drs1060500387
GWAS Ctlgrs1060500387
Max Magnitude0
ClinVar
Risk rs1060500387(-;-)
Alt rs1060500387(-;-)
Reference Rs1060500387(AG;AG)
Significance Pathogenic
Disease Neurofibromatosis Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29685586_29685587delAG
CLNSRC
CLNACC RCV000471092.1, RCV000492474.1,