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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: 325

Gene

GeneSubmissionsLast Updated
ABCC92Sep 27, 2017
ACADVL1Sep 27, 2017
ACTC12Jan 31, 2022
ACTN22Jan 31, 2022
ACVRL11Jan 31, 2022
AGL5Sep 27, 2017
AKAP91Sep 27, 2017
ALMS15Sep 27, 2017
ANK22Sep 27, 2017
APOB11Jan 31, 2022
BAG32Jan 31, 2022
CBL1Sep 27, 2017
CCDC401Sep 27, 2017
COL3A11Jan 31, 2022
CPT22Sep 27, 2017
CTNNA31Sep 27, 2017
DES8Jan 31, 2022
DMD6Sep 27, 2017
DSC24Jan 31, 2022
DSG24Jan 31, 2022
DSP13Jan 31, 2022
ELAC21Sep 27, 2017
ENG2Jan 31, 2022
F21Jan 31, 2022
F51Jan 31, 2022
FBN12Jan 31, 2022
FKRP6Sep 27, 2017
FLNC23Jan 31, 2022
FLNC-AS112Jan 31, 2022
GAA12Sep 27, 2017
GATA45Sep 27, 2017
GATAD11Sep 27, 2017
GJD2-DT2Jan 31, 2022
HCN43Sep 27, 2017
JPH21Sep 27, 2017
JUP6Jan 31, 2022
LAMA45Sep 27, 2017
LDLR2Jan 31, 2022
LDLRAP11Sep 27, 2017
LMNA5Jan 31, 2022
LOC1101212691Jan 31, 2022
MHRT1Jan 31, 2022
MTO12Sep 27, 2017
MYBPC311Jan 31, 2022
MYH111Jan 31, 2022
MYH63Sep 27, 2017
MYH727Jan 31, 2022
MYL31Sep 27, 2017
MYLK9Jan 31, 2022
MYPN1Sep 27, 2017
NDE11Jan 31, 2022
NF11Sep 27, 2017
PCSK94Jan 31, 2022
PKP26Sep 27, 2017
PRKG12Jan 31, 2022
PROC3Jan 31, 2022
PTPN119Sep 27, 2017
RBM206Jan 31, 2022
RYR215Jan 31, 2022
SCN10A2Sep 27, 2017
SCN1B4Sep 27, 2017
SCN5A5Jan 31, 2022
SLC22A53Sep 27, 2017
SLMAP1Sep 27, 2017
SMAD31Jan 31, 2022
SNTA14Sep 27, 2017
SOS12Sep 27, 2017
SOS21Sep 27, 2017
TMEM431Jan 31, 2022
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 cardiomyopathy with woolly hair and keratoderma2Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 101Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 112Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 121Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 131Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 22Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 82Sep 27, 2017
Arrhythmogenic right ventricular dysplasia 91Sep 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
Autosomal recessive limb-girdle muscular dystrophy type 2I3Sep 27, 2017
Autosomal recessive limb-girdle muscular dystrophy type 2J12Sep 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
CBL-related disorder1Sep 27, 2017
Cardiac arrhythmia, ankyrin-B-related2Sep 27, 2017
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis2Sep 27, 2017
Cardiomyopathy, familial restrictive, 31Sep 27, 2017
Carnitine palmitoyl transferase II deficiency, neonatal form2Sep 27, 2017
Carnitine palmitoyl transferase II deficiency, severe infantile form2Sep 27, 2017
Catecholaminergic polymorphic ventricular tachycardia 12Sep 27, 2017
Combined oxidative phosphorylation defect type 171Sep 27, 2017
Desmin-related myofibrillar myopathy2Sep 27, 2017
Developmental and epileptic encephalopathy, 521Sep 27, 2017
Dilated cardiomyopathy 1BB1Sep 27, 2017
Dilated cardiomyopathy 1D1Sep 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 2B1Sep 27, 2017
Dilated cardiomyopathy 3B2Sep 27, 2017
Distal myopathy with posterior leg and anterior hand involvement3Sep 27, 2017
Duchenne muscular dystrophy8Sep 27, 2017
Familial atrial fibrillation1Sep 27, 2017
Familial hypobetalipoproteinemia 14Sep 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
Hypercholesterolemia, autosomal dominant, type B3Sep 27, 2017
Hypercholesterolemia, familial, 11Sep 27, 2017
Hypercholesterolemia, familial, 41Sep 27, 2017
Hypertrichotic osteochondrodysplasia Cantu type1Sep 27, 2017
Hypertrophic cardiomyopathy2Sep 27, 2017
Hypertrophic cardiomyopathy 111Sep 27, 2017
Hypertrophic cardiomyopathy 131Sep 27, 2017
Hypertrophic cardiomyopathy 141Sep 27, 2017
Hypertrophic cardiomyopathy 151Sep 27, 2017
Hypertrophic cardiomyopathy 171Sep 27, 2017
Hypertrophic cardiomyopathy 21Sep 27, 2017
Hypertrophic cardiomyopathy 263Sep 27, 2017
Hypertrophic cardiomyopathy 31Sep 27, 2017
Hypertrophic cardiomyopathy 45Sep 27, 2017
Hypertrophic cardiomyopathy 81Sep 27, 2017
LEOPARD syndrome 13Sep 27, 2017
Left ventricular noncompaction3Sep 27, 2017
Left ventricular noncompaction 102Sep 27, 2017
Long QT syndrome 111Sep 27, 2017
Long QT syndrome 121Sep 27, 2017
MYH7-related skeletal myopathy3Sep 27, 2017
Metachondromatosis3Sep 27, 2017
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency2Sep 27, 2017
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A51Sep 27, 2017
Muscular dystrophy-dystroglycanopathy type B51Sep 27, 2017
Myofibrillar myopathy 53Sep 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
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
not provided2Jan 31, 2022
not specified102Jan 31, 2022
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