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rs267606605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606605(-;-)
Make rs267606605(-;T)
Make rs267606605(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position31327699
GeneNF1
is asnp
is mentioned by
dbSNPrs267606605
ebirs267606605
HLIrs267606605
Exacrs267606605
Varsomers267606605
Maprs267606605
PheGenIrs267606605
hapmaprs267606605
1000 genomesrs267606605
hgdprs267606605
ensemblrs267606605
gopubmedrs267606605
geneviewrs267606605
scholarrs267606605
googlers267606605
pharmgkbrs267606605
gwascentralrs267606605
openSNPrs267606605
23andMers267606605
23andMe allrs267606605
SNP Nexus

SNPshotrs267606605
SNPdbers267606605
MSV3drs267606605
GWAS Ctlgrs267606605
Max Magnitude0
ClinVar
Risk rs267606605(T;T)
Alt rs267606605(T;T)
Reference rs267606605(;)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29654717dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000391.5,