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

rs878853865

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853865(C;T)
Make rs878853865(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31206360
GeneNF1
is asnp
is mentioned by
dbSNPrs878853865
ebirs878853865
HLIrs878853865
Exacrs878853865
Varsomers878853865
Maprs878853865
PheGenIrs878853865
hapmaprs878853865
1000 genomesrs878853865
hgdprs878853865
ensemblrs878853865
gopubmedrs878853865
geneviewrs878853865
scholarrs878853865
googlers878853865
pharmgkbrs878853865
gwascentralrs878853865
openSNPrs878853865
23andMers878853865
23andMe allrs878853865
SNP Nexus

SNPshotrs878853865
SNPdbers878853865
MSV3drs878853865
GWAS Ctlgrs878853865
Max Magnitude0
ClinVar
Risk rs878853865(T;T)
Alt rs878853865(T;T)
Reference rs878853865(C;C)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29533378C>T
CLNSRC
CLNACC RCV000229618.1,