RS387907141 ARID1B

Health Risk Chr 6:157181137
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What This Variant Does
"CLNSIG=5
Associated Conditions
Coffin-Siris syndrome 1
ARID1B-related BAFopathy
Autosomal dominant ARID1B-related disorders
Coffin-Siris syndrome 1
ARID1B-related BAFopathy
Autosomal dominant ARID1B-related disorders
Other Variants in ARID1B
rs387907140 rs876657379 rs876657380 rs748363079 rs387907142 rs876657381 rs387907143 rs387907144 rs876657382 rs587779742
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