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rs786204059

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786204059(-;-)
Make rs786204059(-;AG)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31223504
GeneNF1
is asnp
is mentioned by
dbSNPrs786204059
ebirs786204059
HLIrs786204059
Exacrs786204059
Varsomers786204059
Maprs786204059
PheGenIrs786204059
hapmaprs786204059
1000 genomesrs786204059
hgdprs786204059
ensemblrs786204059
gopubmedrs786204059
geneviewrs786204059
scholarrs786204059
googlers786204059
pharmgkbrs786204059
gwascentralrs786204059
openSNPrs786204059
23andMers786204059
23andMe allrs786204059
SNP Nexus

SNPshotrs786204059
SNPdbers786204059
MSV3drs786204059
GWAS Ctlgrs786204059
Max Magnitude0
ClinVar
Risk rs786204059(;)
Alt rs786204059(;)
Reference rs786204059(AG;AG)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29550522_29550523delAG
CLNSRC
CLNACC RCV000167922.1,