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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADGRG2
(T691A +7 more)
Single nucleotide variant
(missense variant)
Vas deferens, congenital bilateral aplasia of, X-linked
GUncertain significance
ADGRG2
(F100fs +7 more)
Deletion
(frameshift variant)
Vas deferens, congenital bilateral aplasia of, X-linked
GLikely pathogenic