RS141993560 SH3PXD2B

Health Risk Chr 5:172339762
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SH3PXD2B
rs794728005 rs794728006 rs267607046 rs775217258 rs367543284 rs797044638 rs199727236 rs369555721 rs886042037 rs140209484
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