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Haplogroup r-l21Haplogroup o-m175Haplogroup r2Haplogroup o-m176Haplogroup i-m253Haplogroup c-m217Haplogroup r-m269Haplogroup e-m2Haplogroup c-v20Haplogroup d-m55Haplogroup e-m96Haplogroup t-m184Haplogroup i-m438Haplogroup n-m231Haplogroup q-m242Haplogroup e-p2Haplogroup j-m172Haplogroup ijkHaplogroup l-m20Haplogroup e-v38Haplogroup k-m9Haplogroup d-cts3946Haplogroup ctHuman mitochondrial dna haplogroupChromosome 17Rag1Rad51Chromosome 16Chromosome 15Chromosome 18HaplotypeChromosome 1Chromosome 21Chromosome 19Chromosome 11Chromosome 3Chromosome 12Chromosome 6Chromosome 13Chromosome 5Chromosome 9Chromosome 20R-spondin 1GenotypeGenetic markerStructural variationChromosome 8Chromosome 2Mannose receptor c-type 1Chromosome 4ChromosomeChromosome 22Men1Human geneticsNeurofibromin 1Rtp3Hla-a*02GenomeFoxm1GeneticsMutationRh blood group systemHuman mitochondrial geneticsHistone h2a.zGenetic variationAutosomeLig4Neuropilin 1Sequestosome 1Pseudoautosomal regionGenome sizeAscl1LocusBrca2Mcm2Chromosome 7Gata3Caveolin 1NucleolinMitochondrial eveMcm6Hla-cLamin b1Hsf1Hnf1aSortilin 1Integrin alpha 2bMyogeninGrowth hormone receptorFormyl peptide receptor 3SpermMicrotubule-associated protein 2PhenotypeGab1ChromatinHaptoglobinCollagen, type i, alpha 2Cd276Integrin alpha 5Integrin alpha v