RS773495153 SLC29A3

Health Risk Chr 10:71362034
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Associated Conditions
H syndrome
Inborn genetic diseases
H syndrome
Inborn genetic diseases
Other Variants in SLC29A3
rs780668 rs121912583 rs267607056 rs121912584 rs869025176 rs869025177 rs267607057 rs267607058 rs796052139 rs387907066
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