RS201921029 CC2D1A

Health Risk Chr 19:13929607
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What This Variant Does
"CLNSIG=5
Associated Conditions
Smith-Magenis Syndrome-like
Inborn genetic diseases
Intellectual disability
autosomal recessive 3
Smith-Magenis Syndrome-like
Inborn genetic diseases
Intellectual disability
autosomal recessive 3
Other Variants in CC2D1A
rs541952457 rs201177183 rs202057391 rs534160840 rs201374643 rs191830054 rs143529486 rs201884654 rs201251295 rs201665826
Ask Dr. Hemsworth about this variant