RS766452597 PIGV

Health Risk Chr 1:26794648
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hyperphosphatasia with intellectual disability syndrome 1
Inborn genetic diseases
Hyperphosphatasia with intellectual disability syndrome 1
Inborn genetic diseases
Other Variants in PIGV
rs139073416 rs267606951 rs267606952 rs387907023 rs376328153 rs146969255 rs769023704 rs886044116 rs148662665 rs142192097
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