RS764571605 SPTB

Health Risk Chr 14:64786986
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SPTB
rs121918645 rs863223302 rs863223303 rs1594753904 rs121918646 rs121918647 rs121918648 rs121918649 rs121918650 rs121918651
Ask Dr. Hemsworth about this variant