"All of Us Research Program, National Institutes of Health"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1486336	NM_001035.3(RYR2):c.12403C>T (p.Arg4135Cys)	LOC126806068, RYR2 (R4135C)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GUncertain significance
Select item 296761	NM_001035.3(RYR2):c.12404G>A (p.Arg4135His)	LOC126806068, RYR2 (R4135H)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GUncertain significance
Select item 1540601	NM_001035.3(RYR2):c.12405C>T (p.Arg4135=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GLikely benign
Select item 1105564	NM_001035.3(RYR2):c.12408C>T (p.Ile4136=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GLikely benign
Select item 565988	NM_001035.3(RYR2):c.12415A>G (p.Met4139Val)	LOC126806068, RYR2 (M4139V)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 3071087	NM_001035.3(RYR2):c.12423C>G (p.Ser4141Arg)	LOC126806068, RYR2 (S4141R)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 3069972	NM_001035.3(RYR2):c.12426C>G (p.Ala4142=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GLikely benign
Select item 201332	NM_001035.3(RYR2):c.12427A>C (p.Lys4143Gln)	LOC126806068, RYR2 (K4143Q)	Single nucleotide variant (missense variant)	Cardiomyopathy +3 more	GUncertain significance
Select item 920547	NM_001035.3(RYR2):c.12435C>T (p.Ile4145=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GLikely benign
Select item 519230	NM_001035.3(RYR2):c.12437A>G (p.Glu4146Gly)	LOC126806068, RYR2 (E4146G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1546398	NM_001035.3(RYR2):c.12447T>C (p.Tyr4149=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GLikely benign
Select item 3073680	NM_001035.3(RYR2):c.12456C>T (p.Ile4152=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GLikely benign
Select item 532407	NM_001035.3(RYR2):c.12471A>G (p.Arg4157=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GLikely benign
Select item 3385855	NM_001035.3(RYR2):c.12488C>T (p.Pro4163Leu)	LOC126806068, RYR2 (P4163L)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 496088	NM_001035.3(RYR2):c.12489C>T (p.Pro4163=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +3 more	GLikely benign
Select item 201183	NM_001035.3(RYR2):c.12492G>A (p.Gln4164=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 924424	NM_001035.3(RYR2):c.12525C>T (p.Asp4175=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GLikely benign
Select item 201401	NM_001035.3(RYR2):c.12526G>A (p.Val4176Met)	LOC126806068, RYR2 (V4176M)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 2188183	NM_001035.3(RYR2):c.12534C>T (p.Asn4178=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GConflicting classifications of pathogenicity
Select item 959953	NM_001035.3(RYR2):c.12535G>A (p.Glu4179Lys)	LOC126806068, RYR2 (E4179K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GUncertain significance
Select item 463557	NM_001035.3(RYR2):c.12540C>T (p.Gly4180=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 499175	NM_001035.3(RYR2):c.12541G>A (p.Gly4181Arg)	LOC126806068, RYR2 (G4181R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 2 +6 more	GUncertain significance
Select item 412823	NM_001035.3(RYR2):c.12549A>G (p.Lys4183=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1298463	NM_001035.3(RYR2):c.12552G>A (p.Glu4184=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GLikely benign
Select item 463559	NM_001035.3(RYR2):c.12579C>T (p.Cys4193=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not specified +4 more	GLikely benign
Select item 2903393	NM_001035.3(RYR2):c.12580G>A (p.Glu4194Lys)	LOC126806068, RYR2 (E4194K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GUncertain significance
Select item 2106586	NM_001035.3(RYR2):c.12588C>T (p.Thr4196=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GLikely benign
Select item 463560	NM_001035.3(RYR2):c.12589A>G (p.Ile4197Val)	LOC126806068, RYR2 (I4197V)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +3 more	GUncertain significance
Select item 3069678	NM_001035.3(RYR2):c.12590T>C (p.Ile4197Thr)	LOC126806068, RYR2 (I4197T)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 380758	NM_001035.3(RYR2):c.12609G>A (p.Ala4203=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not provided +5 more	GLikely benign
Select item 227907	NM_001035.3(RYR2):c.12609G>T (p.Ala4203=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +5 more	GBenign/Likely benign
Select item 1763212	NM_001035.3(RYR2):c.12612T>C (p.Ala4204=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 918469	NM_001035.3(RYR2):c.12621G>A (p.Ser4207=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 263346	NM_001035.3(RYR2):c.12627G>A (p.Ser4209=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 3070495	NM_001035.3(RYR2):c.12636C>G (p.Asn4212Lys)	LOC126806068, RYR2 (N4212K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 2774396	NM_001035.3(RYR2):c.12636C>A (p.Asn4212Lys)	LOC126806068, RYR2 (N4212K)	Single nucleotide variant (missense variant)	Cardiomyopathy +1 more	GUncertain significance
Select item 1172423	NM_001035.3(RYR2):c.12637G>A (p.Glu4213Lys)	LOC126806068, RYR2 (E4213K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 1003245	NM_001035.3(RYR2):c.12638A>G (p.Glu4213Gly)	LOC126806068, RYR2 (E4213G)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GConflicting classifications of pathogenicity
Select item 921371	NM_001035.3(RYR2):c.12639G>C (p.Glu4213Asp)	LOC126806068, RYR2 (E4213D)	Single nucleotide variant (missense variant)	Cardiomyopathy +2 more	GUncertain significance
Select item 2099802	NM_001035.3(RYR2):c.12647C>T (p.Ala4216Val)	LOC126806068, RYR2 (A4216V)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GConflicting classifications of pathogenicity
Select item 1763746	NM_001035.3(RYR2):c.12647C>A (p.Ala4216Glu)	LOC126806068, RYR2 (A4216E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 496089	NM_001035.3(RYR2):c.12648G>A (p.Ala4216=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign/Likely benign
Select item 568576	NM_001035.3(RYR2):c.12655G>A (p.Glu4219Lys)	LOC126806068, RYR2 (E4219K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GUncertain significance
Select item 924009	NM_001035.3(RYR2):c.12658G>A (p.Glu4220Lys)	LOC126806068, RYR2 (E4220K)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +3 more	GUncertain significance
Select item 919135	NM_001035.3(RYR2):c.12660A>C (p.Glu4220Asp)	LOC126806068, RYR2 (E4220D)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 3072360	NM_001035.3(RYR2):c.12663C>A (p.Ser4221Arg)	LOC126806068, RYR2 (S4221R)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 1332236	NM_001035.3(RYR2):c.12664G>A (p.Glu4222Lys)	LOC126806068, RYR2 (E4222K)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 792314	NM_001035.3(RYR2):c.12666G>A (p.Glu4222=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GLikely benign
Select item 2725621	NM_001035.3(RYR2):c.12667A>G (p.Lys4223Glu)	LOC126806068, RYR2 (K4223E)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GUncertain significance
Select item 749196	NM_001035.3(RYR2):c.12669G>A (p.Lys4223=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +4 more	GBenign/Likely benign
Select item 923421	NM_001035.3(RYR2):c.12674G>A (p.Arg4225Lys)	LOC126806068, RYR2 (R4225K)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 3070897	NM_001035.3(RYR2):c.12677C>T (p.Pro4226Leu)	LOC126806068, RYR2 (P4226L)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 2774398	NM_001035.3(RYR2):c.12678G>A (p.Pro4226=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GLikely benign
Select item 629381	NM_001035.3(RYR2):c.12678G>T (p.Pro4226=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +2 more	GLikely benign
Select item 3074137	NM_001035.3(RYR2):c.12687G>A (p.Gln4229=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GLikely benign
Select item 1370725	NM_001035.3(RYR2):c.12692C>A (p.Pro4231Gln)	LOC126806068, RYR2 (P4231Q)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GUncertain significance
Select item 923238	NM_001035.3(RYR2):c.12693G>A (p.Pro4231=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +3 more	GLikely benign
Select item 1492959	NM_001035.3(RYR2):c.12697A>G (p.Met4233Val)	LOC126806068, RYR2 (M4233V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 201341	NM_001035.3(RYR2):c.12700G>A (p.Ala4234Thr)	LOC126806068, RYR2 (A4234T)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +3 more	GUncertain significance
Select item 43721	NM_001035.3(RYR2):c.12705C>T (p.Phe4235=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +5 more	GConflicting classifications of pathogenicity
Select item 706617	NM_001035.3(RYR2):c.12715C>T (p.Leu4239=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GLikely benign
Select item 1765515	NM_001035.3(RYR2):c.12717G>C (p.Leu4239=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 382856	NM_001035.3(RYR2):c.12720G>C (p.Thr4240=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GLikely benign
Select item 763547	NM_001035.3(RYR2):c.12732C>G (p.Ala4244=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2058998	NM_001035.3(RYR2):c.12735G>A (p.Leu4245=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GLikely benign
Select item 1572140	NM_001035.3(RYR2):c.12741G>A (p.Ala4247=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GLikely benign
Select item 1315962	NM_001035.3(RYR2):c.12752A>G (p.Asn4251Ser)	LOC126806068, RYR2 (N4251S)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +2 more	GConflicting classifications of pathogenicity
Select item 3385856	NM_001035.3(RYR2):c.12756C>G (p.Ile4252Met)	LOC126806068, RYR2 (I4252M)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 922515	NM_001035.3(RYR2):c.12770G>A (p.Arg4257Gln)	LOC126806068, RYR2 (R4257Q)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 2 +4 more	GUncertain significance
Select item 2723022	NM_001035.3(RYR2):c.12780T>C (p.Ser4260=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +2 more	GLikely benign
Select item 3072584	NM_001035.3(RYR2):c.12781C>T (p.Leu4261=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 920833	NM_001035.3(RYR2):c.12795G>A (p.Lys4265=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +2 more	GLikely benign
Select item 3071827	NM_001035.3(RYR2):c.12796A>C (p.Lys4266Gln)	LOC126806068, RYR2 (K4266Q)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 3074482	NM_001035.3(RYR2):c.12812T>G (p.Val4271Gly)	LOC126806068, RYR2 (V4271G)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 3074859	NM_001035.3(RYR2):c.12814A>G (p.Lys4272Glu)	LOC126806068, RYR2 (K4272E)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 3070904	NM_001035.3(RYR2):c.12821T>C (p.Met4274Thr)	LOC126806068, RYR2 (M4274T)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 3074009	NM_001035.3(RYR2):c.12835A>G (p.Met4279Val)	LOC126806068, RYR2 (M4279V)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 920728	NM_001035.3(RYR2):c.12840C>A (p.Val4280=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +1 more	GLikely benign
Select item 2198767	NM_001035.3(RYR2):c.12845C>T (p.Ala4282Val)	LOC126806068, RYR2 (A4282V)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GConflicting classifications of pathogenicity
Select item 201185	NM_001035.3(RYR2):c.12858C>T (p.Ser4286=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 165127	NM_001035.3(RYR2):c.12859T>C (p.Tyr4287His)	LOC126806068, RYR2 (Y4287H)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GConflicting classifications of pathogenicity
Select item 3069303	NM_001035.3(RYR2):c.12862T>C (p.Trp4288Arg)	LOC126806068, RYR2 (W4288R)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 1014648	NM_001035.3(RYR2):c.12865A>G (p.Ser4289Gly)	LOC126806068, RYR2 (S4289G)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GConflicting classifications of pathogenicity
Select item 3385857	NM_001035.3(RYR2):c.12876G>C (p.Met4292Ile)	LOC126806068, RYR2 (M4292I)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 2047554	NM_001035.3(RYR2):c.12880C>T (p.Leu4294Phe)	LOC126806068, RYR2 (L4294F)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +1 more	GUncertain significance
Select item 463561	NM_001035.3(RYR2):c.12893T>C (p.Val4298Ala)	LOC126806068, RYR2 (V4298A)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GUncertain significance
Select item 3071639	NM_001035.3(RYR2):c.12900C>T (p.Ser4300=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 793682	NM_001035.3(RYR2):c.12906C>T (p.Phe4302=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiomyopathy +2 more	GLikely benign
Select item 1442730	NM_001035.3(RYR2):c.12913T>C (p.Phe4305Leu)	LOC126806068, RYR2 (F4305L)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GUncertain significance
Select item 927712	NM_001035.3(RYR2):c.12920G>A (p.Arg4307His)	LOC126806068, RYR2 (R4307H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 1094121	NM_001035.3(RYR2):c.12927T>A (p.Ile4309=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia +2 more	GLikely benign
Select item 3073088	NM_001035.3(RYR2):c.12929G>T (p.Cys4310Phe)	LOC126806068, RYR2 (C4310F)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 412824	NM_001035.3(RYR2):c.12939G>C (p.Leu4313=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 451678	NM_001035.3(RYR2):c.12944G>A (p.Gly4315Glu)	LOC126806068, RYR2 (G4315E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GUncertain significance
Select item 700384	NM_001035.3(RYR2):c.12954C>T (p.Leu4318=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 3074312	NM_001035.3(RYR2):c.12955G>A (p.Val4319Ile)	LOC126806068, RYR2 (V4319I)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia	GUncertain significance
Select item 178126	NM_001035.3(RYR2):c.12957C>T (p.Val4319=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	not specified +5 more	GLikely benign
Select item 707417	NM_001035.3(RYR2):c.12960A>G (p.Glu4320=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GLikely benign
Select item 3073032	NM_001035.3(RYR2):c.12963T>C (p.Gly4321=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia	GLikely benign
Select item 3001458	NM_001035.3(RYR2):c.12966T>A (p.Ala4322=)	LOC126806068, RYR2	Single nucleotide variant (synonymous variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GLikely benign

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