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SNP information rs10965235

Normal allele: CC

A major genetic variant in CDKN2B underlying endometriosis risk.

Polymorphism rs10965235 is related to topics like this:

Endometriosis


Research and publications:

  20601957   A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese.

  21151130   Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.

  23963167   Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.

  23982303   The future for genetic studies in reproduction.

  24676469   Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets.

  24875940   Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population.

  25154675   Association of CDKN2B-AS and WNT4 genetic polymorphisms in Korean patients with endometriosis.

  27055116   Allelic Imbalance in Regulation of ANRIL through Chromatin Interaction at 9p21 Endometriosis Risk Locus.

  27233752   Association of Endometriosis-Associated Genetic Polymorphisms From Genome-Wide Association Studies With Ovarian Endometriosis in a Chinese Population.

  30988702   Defining the genetic profile of endometriosis.

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