RS80356555 VCAN

Health Risk Chr 5:83537005
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What This Variant Does
"Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner sy...
Associated Conditions
Wagner disease
Retinal dystrophy
Inborn genetic diseases
Wagner disease
Wagner disease
Wagner disease
Retinal dystrophy
Inborn genetic diseases
Wagner disease
Wagner disease
Other Variants in VCAN
rs80356554 rs80356556 rs80356553 rs397515437 rs536465380 rs80028865 rs727504214 rs143393049 rs146560021 rs144610900
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