RS587777612 SH2D1A

Health Risk Chr X:124346784
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What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked lymphoproliferative disease due to SH2D1A deficiency
X-linked lymphoproliferative disease due to SH2D1A deficiency
Other Variants in SH2D1A
rs111033623 rs111033628 rs2522814882 rs111033624 rs1603238847 rs111033625 rs111033626 rs1603236465 rs111033629 rs111033630
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