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rs9907627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9907627(A;A)
Make rs9907627(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position31232140
GeneNF1
is asnp
is mentioned by
dbSNPrs9907627
ebirs9907627
HLIrs9907627
Exacrs9907627
Varsomers9907627
Maprs9907627
PheGenIrs9907627
hapmaprs9907627
1000 genomesrs9907627
hgdprs9907627
ensemblrs9907627
gopubmedrs9907627
geneviewrs9907627
scholarrs9907627
googlers9907627
pharmgkbrs9907627
gwascentralrs9907627
openSNPrs9907627
23andMers9907627
23andMe allrs9907627
SNP Nexus

SNPshotrs9907627
SNPdbers9907627
MSV3drs9907627
GWAS Ctlgrs9907627
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene NF1
allele A
frequency 0
sift AFFECT FUNCTION
HuRef 1103645305643
Disease Association Defects in NF1 are a cause of familial spinal neurofibromatosis (spinal NF) (MIM:162210). Familial spinal NF is considered to be an alternative form of neurofibromatosis, showing multiple spinal tumors.