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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861897, MHRT
+1 more
(K1729del)
Microsatellite
(non-coding transcript variant +1 more)
Cardiovascular phenotype
+2 more
GPathogenic
MHRT, LOC126861897
+1 more
(K1617del)
Microsatellite
(inframe_deletion +1 more)
not provided
+3 more
GPathogenic/Likely pathogenic
LOC126861897, MHRT
+1 more
(R1560P)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GLikely pathogenic
MHRT, MYH7
(L1453P)
Single nucleotide variant
(non-coding transcript variant +1 more)
Hypertrophic cardiomyopathy
GPathogenic
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