Phosphorus, Inc., Phosphorus

General information

Phosphorus, Inc., Phosphorus

25 W 26th st.
New York
New York
United States - 10001
https://www.phosphorus.com
Organization ID: 506098

Personnel

Assertion criteria

Level: Assertion criteria provided

Summary of submissions to ClinVar

Total submissions: 221

Gene

GeneSubmissionsLast Updated
ABCC92Sep 27, 2017
ACADVL1Sep 27, 2017
AGL5Sep 27, 2017
AKAP91Sep 27, 2017
ALMS15Sep 27, 2017
ANK22Sep 27, 2017
APOB7Sep 27, 2017
CBL1Sep 27, 2017
CCDC401Sep 27, 2017
CPT22Sep 27, 2017
CTNNA31Sep 27, 2017
DES3Sep 27, 2017
DMD6Sep 27, 2017
DSC22Sep 27, 2017
DSG22Sep 27, 2017
DSP6Sep 27, 2017
ELAC21Sep 27, 2017
FKRP6Sep 27, 2017
FLNC13Sep 27, 2017
FLNC-AS18Sep 27, 2017
GAA12Sep 27, 2017
GATA45Sep 27, 2017
GATAD11Sep 27, 2017
HCN43Sep 27, 2017
JPH21Sep 27, 2017
JUP1Sep 27, 2017
LAMA45Sep 27, 2017
LDLR1Sep 27, 2017
LDLRAP11Sep 27, 2017
MTO12Sep 27, 2017
MYBPC37Sep 27, 2017
MYH63Sep 27, 2017
MYH723Sep 27, 2017
MYL31Sep 27, 2017
MYPN1Sep 27, 2017
NF11Sep 27, 2017
PKP26Sep 27, 2017
PTPN119Sep 27, 2017
RYR26Sep 27, 2017
SCN10A2Sep 27, 2017
SCN1B4Sep 27, 2017
SLC22A53Sep 27, 2017
SLMAP1Sep 27, 2017
SNTA14Sep 27, 2017
SOS12Sep 27, 2017
SOS21Sep 27, 2017
TMPO2Sep 27, 2017
TNNC12Sep 27, 2017
TNNT23Sep 27, 2017
TPM11Sep 27, 2017
TRPM41Sep 27, 2017
TTN37Sep 27, 2017
TTN-AS19Sep 27, 2017
TXNRD21Sep 27, 2017
VCL2Sep 27, 2017

Condition

NameSubmissionsLast Updated
Alstrom syndrome5Sep 27, 2017
Arrhythmogenic right ventricular cardiomyopathy, type 101Sep 27, 2017
Arrhythmogenic right ventricular cardiomyopathy, type 112Sep 27, 2017
Arrhythmogenic right ventricular cardiomyopathy, type 121Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 82Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 91Sep 27, 2017
Arrhythmogenic right ventricular dysplasia, familial, 131Sep 27, 2017
Arrhythmogenic right ventricular dysplasia, familial, 22Sep 27, 2017
Atrial fibrillation, familial, 131Sep 27, 2017
Atrial septal defect 21Sep 27, 2017
Atrial septal defect 31Sep 27, 2017
Atrioventricular septal defect 41Sep 27, 2017
Becker muscular dystrophy2Sep 27, 2017
Brugada syndrome5Sep 27, 2017
Brugada syndrome 51Sep 27, 2017
Brugada syndrome 81Sep 27, 2017
Brugada syndrome 91Sep 27, 2017
Cardiac arrhythmia, ankyrin B-related2Sep 27, 2017
Cardiomyopathy, dilated, 2b1Sep 27, 2017
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis2Sep 27, 2017
Cardiomyopathy, familial hypertrophic, 263Sep 27, 2017
Carnitine palmitoyltransferase II deficiency, infantile2Sep 27, 2017
Carnitine palmitoyltransferase II deficiency, lethal neonatal2Sep 27, 2017
Catecholaminergic polymorphic ventricular tachycardia type 12Sep 27, 2017
Combined oxidative phosphorylation deficiency 102Sep 27, 2017
Combined oxidative phosphorylation deficiency 171Sep 27, 2017
Congenital muscular dystrophy-dystroglycanopathy (with or without mental retardation) type B51Sep 27, 2017
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A51Sep 27, 2017
Dilated cardiomyopathy 1BB1Sep 27, 2017
Dilated cardiomyopathy 1EE1Sep 27, 2017
Dilated cardiomyopathy 1G12Sep 27, 2017
Dilated cardiomyopathy 1I1Sep 27, 2017
Dilated cardiomyopathy 1JJ1Sep 27, 2017
Dilated cardiomyopathy 1KK1Sep 27, 2017
Dilated cardiomyopathy 1S3Sep 27, 2017
Dilated cardiomyopathy 1W1Sep 27, 2017
Dilated cardiomyopathy 1Z1Sep 27, 2017
Dilated cardiomyopathy 3B2Sep 27, 2017
Dilated cardiomyopathy with woolly hair and keratoderma2Sep 27, 2017
Duchenne muscular dystrophy8Sep 27, 2017
Epileptic encephalopathy, early infantile, 521Sep 27, 2017
Familial atrial fibrillation1Sep 27, 2017
Familial hypercholesterolemia 11Sep 27, 2017
Familial hypercholesterolemia 23Sep 27, 2017
Familial hypercholesterolemia 41Sep 27, 2017
Familial hypertrophic cardiomyopathy 111Sep 27, 2017
Familial hypertrophic cardiomyopathy 131Sep 27, 2017
Familial hypertrophic cardiomyopathy 141Sep 27, 2017
Familial hypertrophic cardiomyopathy 151Sep 27, 2017
Familial hypertrophic cardiomyopathy 171Sep 27, 2017
Familial hypertrophic cardiomyopathy 21Sep 27, 2017
Familial hypertrophic cardiomyopathy 31Sep 27, 2017
Familial hypertrophic cardiomyopathy 45Sep 27, 2017
Familial hypertrophic cardiomyopathy 81Sep 27, 2017
Familial restrictive cardiomyopathy 31Sep 27, 2017
Generalized epilepsy with febrile seizures plus, type 11Sep 27, 2017
Glycogen storage disease type III5Sep 27, 2017
Glycogen storage disease, type II12Sep 27, 2017
Hypertrichotic osteochondrodysplasia Cantu type1Sep 27, 2017
Hypertrophic cardiomyopathy2Sep 27, 2017
Hypobetalipoproteinemia, familial, 14Sep 27, 2017
LEOPARD syndrome 13Sep 27, 2017
Left ventricular noncompaction3Sep 27, 2017
Left ventricular noncompaction 102Sep 27, 2017
Left ventricular noncompaction 61Sep 27, 2017
Limb-girdle muscular dystrophy, type 2J12Sep 27, 2017
Limb-girdle muscular dystrophy-dystroglycanopathy, type C53Sep 27, 2017
Long QT syndrome 111Sep 27, 2017
Long QT syndrome 121Sep 27, 2017
Metachondromatosis3Sep 27, 2017
Muscular dystrophy, limb-girdle, type 2R1Sep 27, 2017
Myofibrillar myopathy 11Sep 27, 2017
Myofibrillar myopathy, filamin C-related3Sep 27, 2017
Myopathy, distal, 13Sep 27, 2017
Myopathy, distal, 43Sep 27, 2017
Myopathy, myosin storage, autosomal recessive3Sep 27, 2017
Myosin storage myopathy3Sep 27, 2017
Neurofibromatosis, type 11Sep 27, 2017
Noonan syndrome 13Sep 27, 2017
Noonan syndrome 42Sep 27, 2017
Noonan syndrome 91Sep 27, 2017
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia1Sep 27, 2017
Primary dilated cardiomyopathy9Sep 27, 2017
Renal carnitine transport defect3Sep 27, 2017
Sick sinus syndrome 2, autosomal dominant1Sep 27, 2017
Sodium channelopathy-related small fiber neuropathy1Sep 27, 2017
Spinocerebellar ataxia type 19/221Sep 27, 2017
Tetralogy of Fallot1Sep 27, 2017
Tibial muscular dystrophy13Sep 27, 2017
Ventricular septal defect 11Sep 27, 2017
Very long chain acyl-CoA dehydrogenase deficiency1Sep 27, 2017
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