RS730882228 SPDL1

Health Risk Chr 5:169604102
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Neonatal death
Severe primary microcephaly
Neonatal death
Severe primary microcephaly
Other Variants in SPDL1
rs34833100 rs61735388
Ask Dr. Hemsworth about this variant