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rs1064792854

From SNPedia
ClinVar
Risk rs1064792854(-;-)
Alt rs1064792854(-;-)
Reference Rs1064792854(GCTCGCTGAGCCAA;GCTCGCTGAGCCAA)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU4F3
CLNDBN Deafness, autosomal dominant 15
Reversed 0
HGVS NC_000005.9:g.145719652_145719665delGCTCGCTGAGCCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000087754.3,