RS797044886 HCFC1

Health Risk Chr X:153950387
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in HCFC1
rs398122908 rs318240758 rs397515485 rs397515486 rs397515487 rs398124206 rs201404751 rs199953428 rs782727601 rs782484757
Ask Dr. Hemsworth about this variant