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A question

I’m talking about genetics here
a variation at a single position in a DNA sequence among individuals. These variations, where one nucleotide (A, T, C, or G) is different from the reference sequence, are the most common type of genetic variation found in humans. SNPs can act as markers for various traits, including disease risk and drug response, making them valuable tools in genetic research and personalized medicine.
 
a variation at a single position in a DNA sequence among individuals. These variations, where one nucleotide (A, T, C, or G) is different from the reference sequence, are the most common type of genetic variation found in humans. SNPs can act as markers for various traits, including disease risk and drug response, making them valuable tools in genetic research and personalized medicine.
They also happens to play a part in oxytocin receptors
 
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