{{Rsnum
|rsid = 9907627
|Gene = NF1
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=17
|position=31232140
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NF1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 0.7 | 99.3
| ASW | 0.0 | 3.6 | 96.4
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 1.0 | 99.0
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 3.5 | 96.5
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=9907627
|allele=A
|frequency=0
|uid=1103645305643
|type=heterozygous_SNP
|hugo=NF1
|ensembl gene=ENSG00000196712
|ensembl transcript=ENST00000358273
|sift=AFFECT FUNCTION
|disease=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.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}