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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SREBF1
(R557C +9 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary mucoepithelial dysplasia
+2 more
GPathogenic
MBTPS2
(E172D)
Single nucleotide variant
(missense variant)
IFAP syndrome 1, with or without BRESHECK syndrome
GUncertain significance
MBTPS2
(G176E)
Single nucleotide variant
(missense variant)
Olmsted syndrome, X-linked
+3 more
GUncertain significance
MBTPS2, YY2
Single nucleotide variant
(5 prime UTR variant +1 more)
IFAP syndrome 1, with or without BRESHECK syndrome
+3 more
GUncertain significance
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