RS202080674 ERCC6

Health Risk Chr 10:49482848
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cockayne syndrome type 2
Inborn genetic diseases
Cockayne syndrome type 2
Inborn genetic diseases
Other Variants in ERCC6
rs121917900 rs121917901 rs121917902 rs387906262 rs2132552521 rs758341467 rs4253208 rs121917903 rs1590474873 rs121917904
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