RS776969714 SEPSECS

Health Risk Chr 4:25145129
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pontocerebellar hypoplasia type 2D
Inborn genetic diseases
Pontoneocerebellar hypoplasia
Pontocerebellar hypoplasia type 2D
Inborn genetic diseases
Pontoneocerebellar hypoplasia
Other Variants in SEPSECS
rs267607036 rs267607035 rs587780457 rs61747281 rs1553878395 rs773876739 rs1057518887 rs757504141 rs200041461 rs1553881510
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