RS879255538 ADGRG2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital bilateral aplasia of vas deferens from CFTR mutation
Vas deferens
congenital bilateral aplasia of
X-linked
Congenital bilateral aplasia of vas deferens from CFTR mutation
Vas deferens
congenital bilateral aplasia of
X-linked
Other Variants in ADGRG2