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rs587781780

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781780(-;-)
Make rs587781780(-;AAT)
Make rs587781780(AAT;AAT)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31325888
GeneNF1
is asnp
is mentioned by
dbSNPrs587781780
ebirs587781780
HLIrs587781780
Exacrs587781780
Varsomers587781780
Maprs587781780
PheGenIrs587781780
hapmaprs587781780
1000 genomesrs587781780
hgdprs587781780
ensemblrs587781780
gopubmedrs587781780
geneviewrs587781780
scholarrs587781780
googlers587781780
pharmgkbrs587781780
gwascentralrs587781780
openSNPrs587781780
23andMers587781780
23andMe allrs587781780
SNP Nexus

SNPshotrs587781780
SNPdbers587781780
MSV3drs587781780
GWAS Ctlgrs587781780
Max Magnitude0
ClinVar
Risk rs587781780(AAT;AAT)
Alt rs587781780(AAT;AAT)
Reference rs587781780(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29652906_29652907insAAT
CLNSRC
CLNACC RCV000130028.2,