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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A2
Single nucleotide variant
(splice donor variant)
Atelosteogenesis type II
+7 more
GPathogenic
SLC26A2
(R178*)
Single nucleotide variant
(nonsense)
Diastrophic dysplasia
+7 more
GPathogenic
SLC26A2
(R279W)
Single nucleotide variant
(missense variant)
not specified
+10 more
GPathogenic/Likely pathogenic
SLC26A2
(V341del)
Microsatellite
(inframe_deletion)
Sulfate transporter-related osteochondrodysplasia
+5 more
GPathogenic/Likely pathogenic
SLC26A2
(C653S)
Single nucleotide variant
(missense variant)
Sulfate transporter-related osteochondrodysplasia
+8 more
GPathogenic/Likely pathogenic
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