RS1057517688 MFSD2A

Health Risk Chr 1:39965333
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 15
primary
autosomal recessive
Microcephaly 15
primary
autosomal recessive
Other Variants in MFSD2A
rs1057517689 rs1057519087 rs571640983 rs1570238098 rs147123833 rs2124782476 rs1278119822 rs758953000 rs374629919 rs199920612
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