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rs878853025

From SNPedia

Orientationplus
Geno Mag Summary
(TCTTA;TCTTA) 0 common in clinvar
Make rs878853025(-;-)
Make rs878853025(-;TCTTA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31338796
GeneNF1
is asnp
is mentioned by
dbSNPrs878853025
ebirs878853025
HLIrs878853025
Exacrs878853025
Varsomers878853025
Maprs878853025
PheGenIrs878853025
hapmaprs878853025
1000 genomesrs878853025
hgdprs878853025
ensemblrs878853025
gopubmedrs878853025
geneviewrs878853025
scholarrs878853025
googlers878853025
pharmgkbrs878853025
gwascentralrs878853025
openSNPrs878853025
23andMers878853025
23andMe allrs878853025
SNP Nexus

SNPshotrs878853025
SNPdbers878853025
MSV3drs878853025
GWAS Ctlgrs878853025
Max Magnitude0
ClinVar
Risk rs878853025(;)
Alt rs878853025(;)
Reference rs878853025(TCTTA;TCTTA)
Significance Pathogenic
Disease not provided
Variation info
Gene NF1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.29665814_29665818delTCTTA
CLNSRC
CLNACC RCV000224607.1,