RS267607046 SH3PXD2B

Health Risk Chr 5:172422445
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What This Variant Does
"CLNSIG=5
Associated Conditions
Frank-Ter Haar syndrome
Inborn genetic diseases
Frank-Ter Haar syndrome
Inborn genetic diseases
Other Variants in SH3PXD2B
rs794728005 rs794728006 rs775217258 rs367543284 rs797044638 rs199727236 rs369555721 rs886042037 rs140209484 rs144228973
Ask Dr. Hemsworth about this variant