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rs863224446

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224446(C;C)
Make rs863224446(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31229465
GeneNF1
is asnp
is mentioned by
dbSNPrs863224446
ebirs863224446
HLIrs863224446
Exacrs863224446
Varsomers863224446
Maprs863224446
PheGenIrs863224446
hapmaprs863224446
1000 genomesrs863224446
hgdprs863224446
ensemblrs863224446
gopubmedrs863224446
geneviewrs863224446
scholarrs863224446
googlers863224446
pharmgkbrs863224446
gwascentralrs863224446
openSNPrs863224446
23andMers863224446
23andMe allrs863224446
SNP Nexus

SNPshotrs863224446
SNPdbers863224446
MSV3drs863224446
GWAS Ctlgrs863224446
Max Magnitude0
ClinVar
Risk rs863224446(C;C)
Alt rs863224446(C;C)
Reference rs863224446(G;G)
Significance Probable-Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29556483G>C
CLNSRC
CLNACC RCV000198059.1,