RS886037894 CIT

Health Risk Chr 12:119832835
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 17
primary
autosomal recessive
Microcephaly 17
primary
autosomal recessive
Other Variants in CIT
rs879253817 rs879255522 rs879255524 rs879255523 rs886037892 rs886037893 rs886037895 rs1057520205 rs771292782 rs201214475
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