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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMC1A
(K1064del +1 more)
Microsatellite
(inframe_deletion)
Congenital muscular hypertrophy-cerebral syndrome
GLikely pathogenic
SMC1A
(Q972R +1 more)
Single nucleotide variant
(missense variant)
Congenital muscular hypertrophy-cerebral syndrome
+9 more
GUncertain significance
SMC1A
(R496H +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
SMC1A
(K362E +1 more)
Single nucleotide variant
(missense variant)
Congenital muscular hypertrophy-cerebral syndrome
GUncertain significance
SMC1A
(K268del +1 more)
Microsatellite
(inframe_deletion)
Congenital muscular hypertrophy-cerebral syndrome
+6 more
GPathogenic
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