List of variants studied for Hypertrophic cardiomyopathy 1 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_033118.4(MYLK2):c.577G>A (p.Ala193Thr)	rs1228303561	0.00001
NM_000257.4(MYH7):c.2546T>C (p.Met849Thr)	rs397516156
NM_000257.4(MYH7):c.2560GAG[1] (p.Glu855del)	rs730880887
NM_000257.4(MYH7):c.3133C>A (p.Arg1045Ser)	rs45611033
NM_032578.4(MYPN):c.304C>G (p.Pro102Ala)	rs749935442
NM_033118.4(MYLK2):c.1420A>G (p.Met474Val)	rs1014399187

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