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rs267606598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606598(A;A)
Make rs267606598(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31337514
GeneNF1
is asnp
is mentioned by
dbSNPrs267606598
ebirs267606598
HLIrs267606598
Exacrs267606598
Varsomers267606598
Maprs267606598
PheGenIrs267606598
hapmaprs267606598
1000 genomesrs267606598
hgdprs267606598
ensemblrs267606598
gopubmedrs267606598
geneviewrs267606598
scholarrs267606598
googlers267606598
pharmgkbrs267606598
gwascentralrs267606598
openSNPrs267606598
23andMers267606598
23andMe allrs267606598
SNP Nexus

SNPshotrs267606598
SNPdbers267606598
MSV3drs267606598
GWAS Ctlgrs267606598
Max Magnitude0
ClinVar
Risk rs267606598(A;A)
Alt rs267606598(A;A)
Reference rs267606598(T;T)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29664532T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000368.3,