RS773398782 HLCS

Health Risk Chr 21:36765148
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What This Variant Does
"CLNSIG=4
Associated Conditions
Holocarboxylase synthetase deficiency
Inborn genetic diseases
Holocarboxylase synthetase deficiency
Inborn genetic diseases
Other Variants in HLCS
rs119103227 rs119103228 rs119103229 rs119103230 rs119103231 rs753887925 rs773102942 rs28934602 rs148709879 rs147474255
Ask Dr. Hemsworth about this variant