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rs587781807

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781807(-;-)
Make rs587781807(-;C)
Make rs587781807(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31226466
GeneNF1
is asnp
is mentioned by
dbSNPrs587781807
ebirs587781807
HLIrs587781807
Exacrs587781807
Varsomers587781807
Maprs587781807
PheGenIrs587781807
hapmaprs587781807
1000 genomesrs587781807
hgdprs587781807
ensemblrs587781807
gopubmedrs587781807
geneviewrs587781807
scholarrs587781807
googlers587781807
pharmgkbrs587781807
gwascentralrs587781807
openSNPrs587781807
23andMers587781807
23andMe allrs587781807
SNP Nexus

SNPshotrs587781807
SNPdbers587781807
MSV3drs587781807
GWAS Ctlgrs587781807
Max Magnitude0
ClinVar
Risk rs587781807(C;C)
Alt rs587781807(C;C)
Reference rs587781807(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Neurofibromatosis
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29553484dupC
CLNSRC
CLNACC RCV000130078.1, RCV000204850.1,