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rs786201367

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201367(C;T)
Make rs786201367(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31357308
GeneNF1
is asnp
is mentioned by
dbSNPrs786201367
ebirs786201367
HLIrs786201367
Exacrs786201367
Varsomers786201367
Maprs786201367
PheGenIrs786201367
hapmaprs786201367
1000 genomesrs786201367
hgdprs786201367
ensemblrs786201367
gopubmedrs786201367
geneviewrs786201367
scholarrs786201367
googlers786201367
pharmgkbrs786201367
gwascentralrs786201367
openSNPrs786201367
23andMers786201367
23andMe allrs786201367
SNP Nexus

SNPshotrs786201367
SNPdbers786201367
MSV3drs786201367
GWAS Ctlgrs786201367
Max Magnitude0
ClinVar
Risk rs786201367(T;T)
Alt rs786201367(T;T)
Reference rs786201367(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Neurofibromatosis
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29684326C>T
CLNSRC
CLNACC RCV000163482.1, RCV000196216.1,