Related gene-specific medical variations for Gene (Select 130066413) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2811169	NM_012469.4(PRPF6):c.71+15G>C	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1965948	NM_012469.4(PRPF6):c.71+18G>A	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1659850	NM_012469.4(PRPF6):c.71+15G>T	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1656109	NM_012469.4(PRPF6):c.71+8C>T	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1425292	NM_012469.4(PRPF6):c.71+6_71+7delinsAA	LOC130066413, PRPF6	Indel (intron variant)	not provided	GUncertain significance
Select item 1113718	NM_012469.4(PRPF6):c.71+19C>G	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 961154	NM_012469.4(PRPF6):c.71+7C>T	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 339463	NM_012469.4(PRPF6):c.71+6G>A	LOC130066413, PRPF6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

ClinVar