RS879255634 B4GALT7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ehlers-Danlos syndrome progeroid type
Inborn genetic diseases
Ehlers-Danlos syndrome
spondylodysplastic type
1
Ehlers-Danlos syndrome progeroid type
Inborn genetic diseases
Ehlers-Danlos syndrome
spondylodysplastic type
1
Other Variants in B4GALT7