RS144346996 PYCR1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Cutis laxa
Inborn genetic diseases
Wiedemann-Rautenstrauch-like progeroid syndrome
Autosomal recessive cutis laxa type 2B
PYCR1-related de Barsy syndrome
PYCR1-related disorder
Cutis laxa
Inborn genetic diseases
Wiedemann-Rautenstrauch-like progeroid syndrome
Autosomal recessive cutis laxa type 2B
PYCR1-related de Barsy syndrome
PYCR1-related disorder
Other Variants in PYCR1