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rs267606610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606610(A;C)
Make rs267606610(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position31343138
GeneNF1
is asnp
is mentioned by
dbSNPrs267606610
ebirs267606610
HLIrs267606610
Exacrs267606610
Varsomers267606610
Maprs267606610
PheGenIrs267606610
hapmaprs267606610
1000 genomesrs267606610
hgdprs267606610
ensemblrs267606610
gopubmedrs267606610
geneviewrs267606610
scholarrs267606610
googlers267606610
pharmgkbrs267606610
gwascentralrs267606610
openSNPrs267606610
23andMers267606610
23andMe allrs267606610
SNP Nexus

SNPshotrs267606610
SNPdbers267606610
MSV3drs267606610
GWAS Ctlgrs267606610
Max Magnitude0
ClinVar
Risk rs267606610(C;C)
Alt rs267606610(C;C)
Reference rs267606610(A;A)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, familial spinal
Reversed 0
HGVS NC_000017.10:g.29670156A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000400.4,