RS876661335 FGFR1

Health Risk Chr 8:38414264
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What This Variant Does
"CLNSIG=4
Associated Conditions
Holoprosencephaly sequence
Holoprosencephaly sequence
Other Variants in FGFR1
rs121909627 rs1586111679 rs1563433902 rs121909628 rs121909629 rs1586287678 rs121909630 rs121909632 rs121909631 rs121909633
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