Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853890

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853890(-;-)
Make rs878853890(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31235944
GeneNF1
is asnp
is mentioned by
dbSNPrs878853890
ebirs878853890
HLIrs878853890
Exacrs878853890
Varsomers878853890
Maprs878853890
PheGenIrs878853890
hapmaprs878853890
1000 genomesrs878853890
hgdprs878853890
ensemblrs878853890
gopubmedrs878853890
geneviewrs878853890
scholarrs878853890
googlers878853890
pharmgkbrs878853890
gwascentralrs878853890
openSNPrs878853890
23andMers878853890
23andMe allrs878853890
SNP Nexus

SNPshotrs878853890
SNPdbers878853890
MSV3drs878853890
GWAS Ctlgrs878853890
Max Magnitude0
ClinVar
Risk rs878853890(;)
Alt rs878853890(;)
Reference rs878853890(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29562962delA
CLNSRC
CLNACC RCV000232703.1,