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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF6
(H401Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ARHGEF6
(T152I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
ARHGEF6
(R121H)
Single nucleotide variant
(5 prime UTR variant +1 more)
ARHGEF6-related condition
+3 more
GBenign/Likely benign
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