RS797044867 COL4A1

Health Risk Chr 13:110178196
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Microangiopathy and leukoencephalopathy
pontine
autosomal dominant
Brain small vessel disease 1 with or without ocular anomalies
COL4A1-related disorder
Inborn genetic diseases
Microangiopathy and leukoencephalopathy
pontine
autosomal dominant
Brain small vessel disease 1 with or without ocular anomalies
COL4A1-related disorder
Other Variants in COL4A1
rs113994112 rs113994109 rs121912857 rs113994103 rs113994111 rs113994113 rs113994104 rs113994105 rs113994106 rs113994108
Ask Dr. Hemsworth about this variant