RS147334255 MN1

Health Risk Chr 22:27750995
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
CEBALID syndrome
MN1 C-terminal truncation (MCTT) syndrome
Inborn genetic diseases
CEBALID syndrome
MN1 C-terminal truncation (MCTT) syndrome
Other Variants in MN1
rs1601319501 rs761317200 rs1601319615 rs1601319538 rs1601319598 rs1601319584 rs1933302820 rs1933378166 rs1932758837 rs1932759453
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