Related gene-specific medical variations for Gene (Select 919) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1281371	NM_198053.3(CD247):c.58+158C>T	CD247, LOC126805905	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237879	NM_198053.3(CD247):c.58+59G>C	CD247, LOC126805905	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1179252	NM_198053.3(CD247):c.163-33G>A	CD247, LOC129931851	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

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