{{Rsnum
|rsid=529156
|Gene=ROS1
|Chromosome=6
|position=117301025
|Orientation=minus
|GMAF=0.1598
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=ROS1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 59.3 | 32.7 | 8.0
| HCB | 68.6 | 29.9 | 1.5
| JPT | 77.0 | 21.2 | 1.8
| YRI | 94.6 | 5.4 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 68.6 | 29.9 | 1.5
| CHD | 74.3 | 22.0 | 3.7
| GIH | 75.2 | 22.8 | 2.0
| LWK | 91.8 | 8.2 | 0.0
| MEX | 74.1 | 22.4 | 3.4
| MKK | 73.1 | 24.4 | 2.6
| TSI | 60.8 | 33.3 | 5.9
| HapMapRevision=28
}}{{Venter SNP
|rsid=529156
|allele=G
|frequency=0.25
|uid=1103652977667
|type=homozygous_SNP
|hugo=ROS1
|ensembl gene=ENSG00000047936
|ensembl transcript=ENST00000368508
|sift=
|disease=A chromosomal aberration involving ROS1 is found in glioblastoma multiform (GBM). An homozygous deletion in chromosome 6q21 results in expression of a GOPC-ROS1 chimeric protein which has a constitutive receptor tyrosine kinase activity.
}}

{{ neighbor
| rsid = 619203
| distance = 4
}}
{{ neighbor
| rsid = 529038
| distance = 45
}}

{{GET Evidence
|gene=ROS1
|aa_change=Lys2228Gln
|aa_change_short=K2228Q
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs529156
|overall_frequency_n=2133
|overall_frequency_d=10758
|overall_frequency=0.198271
|n_genomes=22
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|nblosum100=-2
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}