RS869312840 CSNK2A1

Health Risk Chr 20:492282
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What This Variant Does
"CLNSIG=5
Associated Conditions
Okur-Chung neurodevelopmental syndrome
Inborn genetic diseases
See cases
Neurodevelopmental delay
Okur-Chung neurodevelopmental syndrome
Inborn genetic diseases
See cases
Neurodevelopmental delay
Other Variants in CSNK2A1
rs869312846 rs869312848 rs869312849 rs869312845 rs886041956 rs1057518092 rs1057524708 rs1064795110 rs1555761969 rs1555762734
Ask Dr. Hemsworth about this variant