{{Rsnum
|rsid=34006675
|Gene=FKTN
|Chromosome=9
|position=105604218
|Orientation=plus
|GMAF=0.03535
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FKTN
}}{{omim
|id=607440
|rsnum=34006675
|variant=0012
}}

{{ population diversity
| geno1 = (A;G)
| geno2 = (G;G)
| geno3 = 
| CEU | 3.3 | 96.7 | 0
| CHB | 0.0 | 100.0 | 0
| JPT | 0.0 | 100.0 | 0
| YRI | 13.3 | 86.7 | 0
}}

{{ClinVar
|rsid=34006675
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=108366499
|CHROM=9
|GMAF=0.0353
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x05016000000015051e110100
|GENEINFO=FKTN:2218
|GENE_NAME=FKTN
|GENE_ID=2218
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.108366499G>A
|CLNORIGIN=1
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.9646; 0.03535
|CLNACC=RCV000003366.1; RCV000079434.1
|CLNDBN=Reclassified - variant of unknown significance; AllHighlyPenetrant
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNSRCID=5720; 607440.0012
|COMMON=1
|Disease=Reclassified - variant of unknown significance; AllHighlyPenetrant
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|CLNSIG=2
}}

{{GET Evidence
|gene=FKTN
|aa_change=Gly125Ser
|aa_change_short=G125S
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=recessive
|quality_scores=Array
|dbsnp_id=rs34006675
|overall_frequency_n=393
|overall_frequency_d=10758
|overall_frequency=0.036531
|n_genomes=3
|n_genomes_annotated=0
|n_haplomes=3
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=1
|qualitycomment_in_silico=Y
|qualityscore_case_control=0
|qualitycomment_case_control=Y
|qualityscore_familial=0
|qualityscore_severity=5
|qualitycomment_severity=Y
|qualityscore_treatability=1
|gene_in_genetests=Y
|in_omim=Y
|pph2_score=0.001
|genetests_testable=Y
|genetests_reviewed=Y
|nblosum100=2
|autoscore=4
|webscore=N
|n_web_uneval=1
|summary_short=This variant was found as a compound heterozygote with a 473-bp deletion in a Spanish individual with Walker-Warburg syndrome
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}