|
Atherosclerotic cardiovascular disease (risk of)
|
9q21.3
|
P273-PCSK5newbasic research
|
€ 1145
|
|
Autism Spectrum Disorder
|
22q13.33
|
P339-SHANK3new
|
€ 1145
|
|
Mismatch repair genes (MMR)
|
MLH1, MSH2, MSH6, MLH3, MSH3
|
ME011-MMRimproved
|
€ 1145
|
|
Mitochondrial maintenance
|
POLG, POLG2, C10orf2 (PEO1), SLC25A4 (ANT1)
|
P010-POLGnew
|
€ 1145
|
|
Myotonia congenita, Thomsen’s disease, Becker’s disease, Andersen-Tawil syndrome
|
CLCN1, KCNJ2
|
P350-CLCN1-KCNJ2new
|
€ 1145
|
|
Neurofibromatosis type 2 (NF2)
|
NF2 22q12
|
P044-NF2improved
|
€ 1145
|
|
Pendred syndrome
|
SLC26A4 7q31
|
P280-SLC26A4improved
|
€ 1145
|
|
Retinitis pigmentosa (RP)
|
CHM-RP2-RPGR
|
P366-CHM-RP2-RPGRnew
|
€ 1145
|
|
Skeletal disorders, Achondrogenesis, Chondrodysplasia, Early onset familial Osteoarthritis, SED congenital, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome, Spondyloepimetaphyseal
|
COL2A1 12q13.11-q13.2
|
P214-COL2A1improved
|
€ 1145
|
|
Sotos syndrome
|
NSD1, 5q35
|
P026-Sotosimproved
|
€ 1145
|
|
Tay-sachs disease
|
HEXA 15q23
|
P199-HEXAimproved
|
€ 1145
|