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rs267606595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606595(A;T)
Make rs267606595(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31334933
GeneNF1
is asnp
is mentioned by
dbSNPrs267606595
ebirs267606595
HLIrs267606595
Exacrs267606595
Varsomers267606595
Maprs267606595
PheGenIrs267606595
hapmaprs267606595
1000 genomesrs267606595
hgdprs267606595
ensemblrs267606595
gopubmedrs267606595
geneviewrs267606595
scholarrs267606595
googlers267606595
pharmgkbrs267606595
gwascentralrs267606595
openSNPrs267606595
23andMers267606595
23andMe allrs267606595
SNP Nexus

SNPshotrs267606595
SNPdbers267606595
MSV3drs267606595
GWAS Ctlgrs267606595
Max Magnitude0
ClinVar
Risk rs267606595(T;T)
Alt rs267606595(T;T)
Reference rs267606595(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29661951A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000363.3,