RS80359861 ESCO2

Health Risk Chr 8:27788003
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What This Variant Does
"Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype corr...
Associated Conditions
Juberg-Hayward syndrome
Roberts-SC phocomelia syndrome
Juberg-Hayward syndrome
Roberts-SC phocomelia syndrome
Other Variants in ESCO2
rs80359868 rs80359849 rs1554554098 rs80359852 rs80359864 rs80359850 rs1554555716 rs80359859 rs80359862 rs80359865
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