RS869025343 NONO

Health Risk Chr X:71297938
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What This Variant Does
"CLNSIG=5
Associated Conditions
Syndromic X-linked intellectual disability 34
Inborn genetic diseases
Syndromic X-linked intellectual disability 34
Inborn genetic diseases
Other Variants in NONO
rs869025344 rs869025345 rs876661316 rs1057518476 rs1057524408 rs1064796806 rs1085307870 rs1114167441 rs1555949215 rs1555950011
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