RS879255522 CIT

Health Risk Chr 12:119822819
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive primary microcephaly
Microcephaly 17
primary
autosomal recessive
Autosomal recessive primary microcephaly
Microcephaly 17
primary
autosomal recessive
Other Variants in CIT
rs879253817 rs879255524 rs879255523 rs886037892 rs886037893 rs886037894 rs886037895 rs1057520205 rs771292782 rs201214475
Ask Dr. Hemsworth about this variant