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rs878853922

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853922(A;G)
Make rs878853922(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31200420
GeneNF1
is asnp
is mentioned by
dbSNPrs878853922
ClinGenrs878853922
ebirs878853922
HLIrs878853922
Exacrs878853922
Varsomers878853922
Maprs878853922
PheGenIrs878853922
hapmaprs878853922
1000 genomesrs878853922
hgdprs878853922
ensemblrs878853922
gopubmedrs878853922
geneviewrs878853922
scholarrs878853922
googlers878853922
pharmgkbrs878853922
gwascentralrs878853922
openSNPrs878853922
23andMers878853922
23andMe allrs878853922
SNP Nexus

SNPshotrs878853922
SNPdbers878853922
MSV3drs878853922
GWAS Ctlgrs878853922
Max Magnitude0
ClinVar
Risk rs878853922(G;G)
Alt rs878853922(G;G)
Reference Rs878853922(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29527438A>G
CLNSRC
CLNACC RCV000227780.1,