RS1057517412 BCS1L

Health Risk Chr 2:218661501
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What This Variant Does
"CLNSIG=4
Associated Conditions
GRACILE syndrome
Inborn genetic diseases
GRACILE syndrome
Inborn genetic diseases
Other Variants in BCS1L
rs121908571 rs121908572 rs121908573 rs121908574 rs28937590 rs121908575 rs121908576 rs121908577 rs121908578 rs121908579
Ask Dr. Hemsworth about this variant