RS886039763 HNRNPH2

Health Risk Chr X:101412604
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
X-linked
syndromic
Bain type
Inborn genetic diseases
Neurodevelopmental disorder
Neurodevelopmental delay
Stereotypic movement disorder
Abnormal facial shape
Intellectual disability
X-linked
syndromic
Bain type
Inborn genetic diseases
Neurodevelopmental disorder
Other Variants in HNRNPH2
rs1555988417 rs886039764 rs1555988404 rs1555988422 rs1555988314 rs1928842837 rs782191163 rs2520984887 rs2520983929 rs2520985089
Ask Dr. Hemsworth about this variant