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Masteriza [31]
2 years ago
10

PLS HELP ASAP 100 POINTS IF YOU ANSWER THE QUESTION,DONT JUST ANSWER FOR THE POINTS I REALLY NEED THIS.

Biology
2 answers:
Kisachek [45]2 years ago
5 0

Answer:

Benefits

Direct-to-consumer genetic testing promotes awareness of genetic diseases.

It provides personalized information about your health, disease risk, and other traits.

It may help you be more proactive about your health.

It does not require approval from a healthcare provider or health insurance company.

It is often less expensive than genetic testing obtained through a healthcare provider.

DNA sample collection is usually simple and noninvasive, and results are available quickly.

Your data is added to a large database that can be used to further medical research. Depending on the company, the database may represent up to several million participants.

Risks and limitations

Tests may not be available for the health conditions or traits that interest you.

This type of testing cannot tell definitively whether you will or will not get a particular disease.

Unexpected information that you receive about your health, family relationships, or ancestry may be stressful or upsetting.

People may make important decisions about disease treatment or prevention based on inaccurate, incomplete, or misunderstood information from their test results.

There is currently little oversight or regulation of testing companies.

Unproven or invalid tests can be misleading. There may not be enough scientific evidence to link a particular genetic variation with a given disease or trait.

Genetic privacy may be compromised if testing companies use your genetic information in an unauthorized way or if your data is stolen.

The results of genetic testing may impact your ability to obtain life, disability, or long-term care insurance.

Explanation:

Zina [86]2 years ago
4 0

Answer:

I would support a similar gene database, but I would make it simpler for consumers, by editing the pages to make the information easier to read.

Explanation:

Hope this helped! :)

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Sickle cell anemia is a recessive trait in humans. In a cross between a father who has sickle cell anemia and a mother who is he
Ghella [55]

Answer:

75% probability

Explanation:

The father have the trait of sickle cell anemia which means he is a sickle cell dominant with a trait of dominant SS ( meaning he has displays the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele i.e homozygous). While the mother is heterogygous which means that she has one abnormal allele of the hemoglobin beta gene represented as As.

Based on this notion, upon crossing of the traits the probabilities are<em> 75% Heterogygous trait and 25% homoxygous traits (i.e As, As, As, SS)</em>. Meaning 75% of the children will be unaffected by the Sickle cell anemia, while 25% will be affected by the anemia.

8 0
3 years ago
Why is it important to use mla format??
ruslelena [56]

Explanation:

Using MLA Style properly makes it easier for readers to navigate and comprehend a text through familiar cues that refer to sources and borrowed information. Editors and instructors also encourage everyone to use the same format so there is consistency of style within a given field.

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finlep [7]
Nope... I don't remember when it did but no
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When pure black hamsters were mated with pure white hamsters, all of the offspring were black. The trait for whiteness would bes
Angelina_Jolie [31]

Answer:

Recessive

Explanation:

All of the offsrping were black so that means black was the dominant gene and white was the recessive

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How do products of meiosis I differ from those of meiosis ll?
VLD [36.1K]
Meiosis I is dedicated to forming two Haploid(half chromosome) cells bby separating each pair of chromosomes (one of each type in each cell) and the recombination, or shuffling of genes on each chromosome with its pair by crossing over, While Meiosis II is meant to split the individual chromatids in the haploid cells to create a total or 4 daughter cells 

Hope this helps! :)

3 0
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