RS312262798 NOTCH2

Health Risk Chr 1:119917763
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What This Variant Does
"CLNSIG=5
Associated Conditions
Alagille syndrome due to a NOTCH2 point mutation
Alagille syndrome due to a NOTCH2 point mutation
Other Variants in NOTCH2
rs111033632 rs1557802353 rs387906746 rs1557801639 rs387906747 rs387906748 rs387906749 rs312262801 rs146014987 rs115013051
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