List of variants reported as likely pathogenic for sudden cardiac failure, infantile

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_176869.3(PPA2):c.514G>A (p.Glu172Lys)	rs146013446	0.00069
NM_176869.3(PPA2):c.683C>T (p.Pro228Leu)	rs138215926	0.00044
NM_176869.3(PPA2):c.380G>T (p.Arg127Leu)	rs139076647	0.00022
NM_176869.3(PPA2):c.476C>T (p.Thr159Met)	rs752062224	0.00005
NM_176869.3(PPA2):c.500C>T (p.Pro167Leu)	rs546693824	0.00001
NM_176869.3(PPA2):c.814C>T (p.His272Tyr)	rs758551684	0.00001
NM_176869.3(PPA2):c.182C>T (p.Ser61Phe)	rs772083375
NM_176869.3(PPA2):c.442A>T (p.Thr148Ser)	rs1187924642
NM_176869.3(PPA2):c.606G>C (p.Trp202Cys)	rs1723387280
NM_176869.3(PPA2):c.938C>A (p.Ser313Ter)	rs151331559

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