TMEM258, transmembrane protein 258, 746

N. diseases: 63; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1382225004
rs1382225004
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
0.800 GeneticVariation UNIPROT
dbSNP: rs1382225004
rs1382225004
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
A 0.800 CausalMutation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C1735886
Disease:
Bland White Garland Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0010417
Disease:
Cryptorchidism
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0032461
Disease:
Polycythemia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4551904
Disease:
Total Anomalous Pulmonary Venous Return 1
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0240635
Disease:
Byzanthine arch palate
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295267
rs1565295267
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0011813
Disease:
Dextrocardia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1565295286
rs1565295286
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4722446
Disease:
ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565295395
rs1565295395
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
AAG 0.700 CausalMutation CLINVAR
dbSNP: rs1565295550
rs1565295550
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs1565304230
rs1565304230
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0018817
Disease:
Atrial Septal Defects
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0013274
Disease:
Patent ductus arteriosus
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0685707
Disease:
Muscular ventricular septum defect
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0152101
Disease:
Hypoplastic Left Heart Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0036400
Disease:
Scimitar Syndrome
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565307564
rs1565307564
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0344760
Disease:
Congenital atresia of mitral valve
G 0.700 CausalMutation CLINVAR
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0265783
Disease:
Congenital hypoplasia of lung
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C4748946
Disease:
CARDIAC-UROGENITAL SYNDROME
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0152101
Disease:
Hypoplastic Left Heart Syndrome
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C1691215
Disease:
Penile hypospadias
CA 0.700 CausalMutation CLINVAR
dbSNP: rs1565308384
rs1565308384
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0221182
Disease:
Chordee
CA 0.700 CausalMutation CLINVAR
dbSNP: rs174537
rs174537
Entrez Id: 745;746
Gene Symbol: MYRF;TMEM258
MYRF;TMEM258
CUI: C0202236
Disease:
Triglycerides measurement
0.800 GeneticVariation GWASDB A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. 19074352 2008