ערכת דנ''א לבריאות של MyHeritage
רק$99
$199
+ shipping
Current List of Conditions and Genes
Your health reports will include:
42 Genetic Risk and Carrier Status ReportsPolygenic risk reports for conditions such as heart disease, breast cancer, and type 2 diabetes (available for people who are of mainly European ancestry)Risk reports for 103 variants on the BRCA1/BRCA2 genes
We are working on adding reports for many more conditions in the next few months.
ערכת דנ''א לבריאות של MyHeritage
רק$99
$199
+ shipping
5 Polygenic Risk Reports
ConditionGenesNumber of variants
- Female breast cancerPolygenicMany
- Heart diseasePolygenicMany
- High blood pressurePolygenicMany
- Obesity and High BMIחדשPolygenicMany
- Type 2 diabetesPolygenicMany
14 Monogenic Risk Reports
ConditionGenesNumber of variants
- Alpha-1 antitrypsin deficiencySERPINA12
- Celiac diseaseHLA-DQA1, HLA-DQB12
- Crohn's diseaseNOD22
- G6PD deficiencyG6PD2
- Hereditary BRCA cancersupdatedBRCA1, BRCA2103
- Hereditary hemochromatosisHFE2
- Hereditary thrombophiliaF2, F5, PROC, PROS14
- Late-onset Alzheimer's diseaseAPOE2
- Late-onset Parkinson's diseaseGBA, LRRK22
- MUTYH-associated colorectal cancerMUTYH4
- Susceptibility to HIV-1 infectionCCR51
- Susceptibility to malignant hyperthermiaRYR11
23 Carrier Status reports
ConditionGenesNumber of variants
- Ataxia-telangiectasia syndromeATM2
- Bardet-Biedl syndrome 2חדשBBS22
- Congenital amegakaryocytic thrombocytopenia (CAMT)חדשMPL1
- Cystic fibrosisCFTR20
- Familial dysautonomiaIKBKAP1
- Familial Mediterranean fever (FMF)MEFV7
- Fanconi anemiaFANCC4
- Gaucher diseaseGBA2
- Glycogen storage disease type 1AG6PC5
- GRACILE syndromeBCS1L1
- Hereditary fructose intoleranceחדשALDOB4
- Joubert syndrome 2חדשTMEM2161
- Limb-girdle muscular dystrophy, type 2DSGCA1
- Mucolipidosis type IV (ML4)MCOLN11
- Niemann-Pick disease, types A and BSMPD14
- Nonsyndromic hearing loss (connexin 26)GJB24
- Rhizomelic chondrodysplasia punctata, type 1PEX71
- Sickle cell anemiaHBB1
- Tay-Sachs diseaseHEXA7
- Tyrosinemia type IחדשFAH4
- Usher syndrome, type 2AUSH2A1
- Usher syndrome, type 3CLRN1 (USH3)2