RS1556226291 SPECC1L

Health Risk Chr 22:24322272
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Associated Conditions
Autosomal dominant Opitz G/BBB syndrome
Autosomal dominant Opitz G/BBB syndrome
Other Variants in SPECC1L
rs190313411 rs200870836 rs143004795 rs2040735453 rs199858278 rs1318284690 rs139099983 rs201626909 rs547014400 rs200239876
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