RS80359847 ESCO2

Health Risk Chr 8:27776614
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What This Variant Does
"CLNSIG=5
Associated Conditions
Roberts-SC phocomelia syndrome
Inborn genetic diseases
Roberts-SC phocomelia syndrome
Inborn genetic diseases
Other Variants in ESCO2
rs80359868 rs80359849 rs1554554098 rs80359852 rs80359864 rs80359850 rs1554555716 rs80359859 rs80359861 rs80359862
Ask Dr. Hemsworth about this variant