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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AR, LOC109504725
(Q63L)
Single nucleotide variant
(missense variant +1 more)
Kennedy disease
+2 more
GUncertain significance
AR, LOC109504725
(Q77*)
Single nucleotide variant
(nonsense +1 more)
Aplasia of the uterus
+3 more
GPathogenic
AR
(E289*)
Single nucleotide variant
(nonsense +1 more)
Androgen resistance syndrome
GPathogenic
AR
Single nucleotide variant
(intron variant)
Malignant tumor of prostate
GUncertain significance
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