RS769987150 SPTBN2

Health Risk Chr 11:66705361
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SPTBN2
rs1941485201 rs121918306 rs146859515 rs397514749 rs373728971 rs786205617 rs148207416 rs150159444 rs200956071 rs797046005
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