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rs878853893

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853893(A;G)
Make rs878853893(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31259068
GeneNF1
is asnp
is mentioned by
dbSNPrs878853893
ebirs878853893
HLIrs878853893
Exacrs878853893
Varsomers878853893
Maprs878853893
PheGenIrs878853893
hapmaprs878853893
1000 genomesrs878853893
hgdprs878853893
ensemblrs878853893
gopubmedrs878853893
geneviewrs878853893
scholarrs878853893
googlers878853893
pharmgkbrs878853893
gwascentralrs878853893
openSNPrs878853893
23andMers878853893
23andMe allrs878853893
SNP Nexus

SNPshotrs878853893
SNPdbers878853893
MSV3drs878853893
GWAS Ctlgrs878853893
Max Magnitude0
ClinVar
Risk rs878853893(G;G)
Alt rs878853893(G;G)
Reference rs878853893(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29586086A>G
CLNSRC
CLNACC RCV000229110.1,