{{Rsnum
|rsid=12635698
|Gene=RFTN1
|Chromosome=3
|position=16366982
|Orientation=plus
|GMAF=0.208
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RFTN1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 26.5 | 72.6
| HCB | 0.0 | 6.6 | 93.4
| JPT | 0.0 | 4.4 | 95.6
| YRI | 34.0 | 47.6 | 18.4
| ASW | 26.3 | 57.9 | 15.8
| CHB | 0.0 | 6.6 | 93.4
| CHD | 0.0 | 6.4 | 93.6
| GIH | 1.0 | 21.8 | 77.2
| LWK | 38.2 | 50.0 | 11.8
| MEX | 0.0 | 12.3 | 87.7
| MKK | 16.7 | 50.0 | 33.3
| TSI | 2.0 | 28.3 | 69.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19553259
|Trait=Obesity (extreme)
|Title=Common BMI-associated variants confer risk of extreme obesity
|RiskAllele=C
|Pval=0.000005
|OR=1.41
|ORtxt=[1.21-1.63]
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12635698
|overall_frequency_n=36
|overall_frequency_d=128
|overall_frequency=0.28125
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=31
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

Occurs within the RFTN1 (Raftlin, lipid raft linker 1) gene

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}