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rs587782819

From SNPedia

Orientationplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs587782819(-;-)
Make rs587782819(-;AAG)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31338803
GeneNF1
is asnp
is mentioned by
dbSNPrs587782819
ebirs587782819
HLIrs587782819
Exacrs587782819
Varsomers587782819
Maprs587782819
PheGenIrs587782819
hapmaprs587782819
1000 genomesrs587782819
hgdprs587782819
ensemblrs587782819
gopubmedrs587782819
geneviewrs587782819
scholarrs587782819
googlers587782819
pharmgkbrs587782819
gwascentralrs587782819
openSNPrs587782819
23andMers587782819
23andMe allrs587782819
SNP Nexus

SNPshotrs587782819
SNPdbers587782819
MSV3drs587782819
GWAS Ctlgrs587782819
Max Magnitude0
ClinVar
Risk rs587782819(;)
Alt rs587782819(;)
Reference rs587782819(AAG;AAG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29665821_29665823delAAG
CLNSRC
CLNACC RCV000132393.2,