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rs267606603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606603(A;A)
Make rs267606603(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position31201486
GeneNF1
is asnp
is mentioned by
dbSNPrs267606603
ebirs267606603
HLIrs267606603
Exacrs267606603
Varsomers267606603
Maprs267606603
PheGenIrs267606603
hapmaprs267606603
1000 genomesrs267606603
hgdprs267606603
ensemblrs267606603
gopubmedrs267606603
geneviewrs267606603
scholarrs267606603
googlers267606603
pharmgkbrs267606603
gwascentralrs267606603
openSNPrs267606603
23andMers267606603
23andMe allrs267606603
SNP Nexus

SNPshotrs267606603
SNPdbers267606603
MSV3drs267606603
GWAS Ctlgrs267606603
Max Magnitude0
ClinVar
Risk rs267606603(A;A)
Alt rs267606603(A;A)
Reference rs267606603(G;G)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, type 1
Reversed 0
HGVS NC_000017.10:g.29528504G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000384.4,