RS386833856 BCS1L

Health Risk Chr 2:218661308
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What This Variant Does
"CLNSIG=4
Associated Conditions
GRACILE syndrome
Inborn genetic diseases
Pili torti-deafness syndrome
GRACILE syndrome
Inborn genetic diseases
Pili torti-deafness syndrome
Other Variants in BCS1L
rs121908571 rs121908572 rs121908573 rs121908574 rs28937590 rs121908575 rs121908576 rs121908577 rs121908578 rs121908579
Ask Dr. Hemsworth about this variant