Related gene-specific medical variations for Gene (Select 4049) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14381	NM_000595.4(LTA):c.-92=	LOC100287329, LTA	Single nucleotide variant (no sequence alteration +1 more)	Leprosy, early-onset, susceptibility to	Grisk factor
Select item 14380	NM_000595.4(LTA):c.-10+90A>G	LOC100287329, LTA	Single nucleotide variant (intron variant)	Myocardial infarction, susceptibility to +1 more	Grisk factor