RS121908047 GALE
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What This Variant Does
"[OMIM:?]
Associated Conditions
Galactosemia III
severe
UDPglucose-4-epimerase deficiency
Inborn genetic diseases
Thrombocytopenia 13
syndromic
Galactosemia III
severe
UDPglucose-4-epimerase deficiency
Inborn genetic diseases
Thrombocytopenia 13
syndromic
Other Variants in GALE