RS879255516 CTCF

Health Risk Chr 16:67628550
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What This Variant Does
"CLNSIG=5
Associated Conditions
CTCF-related neurodevelopmental disorder
CTCF-related syndromic intellectual disability
Inborn genetic diseases
Intellectual disability
CTCF-related neurodevelopmental disorder
CTCF-related syndromic intellectual disability
Inborn genetic diseases
Intellectual disability
Other Variants in CTCF
rs879255570 rs879255571 rs148681672 rs886039600 rs886041997 rs886041901 rs1064796062 rs1131691283 rs1555535156 rs1555535157
Ask Dr. Hemsworth about this variant