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rs587781577

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781577(C;C)
Make rs587781577(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position31227217
GeneNF1
is asnp
is mentioned by
dbSNPrs587781577
ebirs587781577
HLIrs587781577
Exacrs587781577
Varsomers587781577
Maprs587781577
PheGenIrs587781577
hapmaprs587781577
1000 genomesrs587781577
hgdprs587781577
ensemblrs587781577
gopubmedrs587781577
geneviewrs587781577
scholarrs587781577
googlers587781577
pharmgkbrs587781577
gwascentralrs587781577
openSNPrs587781577
23andMers587781577
23andMe allrs587781577
SNP Nexus

SNPshotrs587781577
SNPdbers587781577
MSV3drs587781577
GWAS Ctlgrs587781577
Max Magnitude0
ClinVar
Risk rs587781577(C;C)
Alt rs587781577(C;C)
Reference rs587781577(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29554235G>C
CLNSRC
CLNACC RCV000129613.1,