RS398122976 STIL

Health Risk Chr 1:47269857
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 7
primary
autosomal recessive
Microcephaly 7
primary
autosomal recessive
Other Variants in STIL
rs121918609 rs199422207 rs199422206 rs3766317 rs149185431 rs75426387 rs188900275 rs587784452 rs200532713 rs149697952
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