RS587777148 KPTN

Health Risk Chr 19:47479918
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What This Variant Does
"CLNSIG=5
Associated Conditions
Macrocephaly-developmental delay syndrome
KPTN-related disorder
Inborn genetic diseases
Macrocephaly-developmental delay syndrome
KPTN-related disorder
Inborn genetic diseases
Other Variants in KPTN
rs2122670288 rs1192367520 rs2122687547 rs1243527780 rs781132082 rs2122687472 rs2515242437 rs1967952850 rs754861924 rs1332315502
Ask Dr. Hemsworth about this variant