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rs267606601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606601(-;-)
Make rs267606601(-;A)
Make rs267606601(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position31358614
GeneNF1
is asnp
is mentioned by
dbSNPrs267606601
ebirs267606601
HLIrs267606601
Exacrs267606601
Varsomers267606601
Maprs267606601
PheGenIrs267606601
hapmaprs267606601
1000 genomesrs267606601
hgdprs267606601
ensemblrs267606601
gopubmedrs267606601
geneviewrs267606601
scholarrs267606601
googlers267606601
pharmgkbrs267606601
gwascentralrs267606601
openSNPrs267606601
23andMers267606601
23andMe allrs267606601
SNP Nexus

SNPshotrs267606601
SNPdbers267606601
MSV3drs267606601
GWAS Ctlgrs267606601
Max Magnitude0
ClinVar
Risk rs267606601(A;A)
Alt rs267606601(A;A)
Reference rs267606601(;)
Significance Pathogenic
Disease Neurofibromatosis
Variation info
Gene NF1
CLNDBN Neurofibromatosis, familial spinal
Reversed 0
HGVS NC_000017.10:g.29685632dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000377.2,