ClinVar Miner

List of variants in gene IMPAD1 reported as likely benign for Chondrodysplasia

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_017813.5(IMPAD1):c.*2608A>C rs17188824
NM_017813.5(IMPAD1):c.*3204A>G rs3739364
NM_017813.5(IMPAD1):c.*4123_*4125del rs143068938
NM_017813.5(IMPAD1):c.*4890C>T rs1044731
NM_017813.5(IMPAD1):c.*5014A>G rs111729642
NM_017813.5(IMPAD1):c.*501_*503TGT[1] rs199901281
NM_017813.5(IMPAD1):c.*5512T>C rs9315
NM_017813.5(IMPAD1):c.*5689dup rs200630025
NM_017813.5(IMPAD1):c.*5730A>G rs80163062
NM_017813.5(IMPAD1):c.*701C>T rs1046636
NM_017813.5(IMPAD1):c.*764C>T rs10003
NM_017813.5(IMPAD1):c.*782G>A rs1046643
NM_017813.5(IMPAD1):c.*980del rs113846940
NM_017813.5(IMPAD1):c.-125C>T rs1057409
NM_017813.5(IMPAD1):c.-169C>T rs1057407

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