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rs587782814

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782814(G;G)
Make rs587782814(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31229204
GeneNF1
is asnp
is mentioned by
dbSNPrs587782814
ebirs587782814
HLIrs587782814
Exacrs587782814
Varsomers587782814
Maprs587782814
PheGenIrs587782814
hapmaprs587782814
1000 genomesrs587782814
hgdprs587782814
ensemblrs587782814
gopubmedrs587782814
geneviewrs587782814
scholarrs587782814
googlers587782814
pharmgkbrs587782814
gwascentralrs587782814
openSNPrs587782814
23andMers587782814
23andMe allrs587782814
SNP Nexus

SNPshotrs587782814
SNPdbers587782814
MSV3drs587782814
GWAS Ctlgrs587782814
Max Magnitude0
ClinVar
Risk rs587782814(G;G)
Alt rs587782814(G;G)
Reference rs587782814(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29556222T>G
CLNSRC
CLNACC RCV000132382.2,