U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCAD1
(S246N +1 more)
Single nucleotide variant
(missense variant +1 more)
Basan syndrome
+3 more
GBenign
SMARCAD1
Single nucleotide variant
(synonymous variant +1 more)
Adermatoglyphia
+3 more
GBenign
SMARCAD1
Single nucleotide variant
(synonymous variant +1 more)
Keratoderma with scleroatrophy of the extremities
+3 more
GBenign
SMARCAD1
(V300A +1 more)
Single nucleotide variant
(missense variant +1 more)
Keratoderma with scleroatrophy of the extremities
+3 more
GBenign
LOC129992843, SMARCAD1
+1 more
Complex
Basan syndrome
GPathogenic
SMARCAD1
Single nucleotide variant
(intron variant)
Basan syndrome
GPathogenic
SMARCAD1
Single nucleotide variant
(intron variant +1 more)
Basan syndrome
+1 more
GPathogenic
Format
Items per page
Sort by
Choose Destination