ClinVar Miner

List of variants in gene SERPINF1 reported as benign for bone development disease

Included ClinVar conditions (614):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_002615.7(SERPINF1):c.963T>C (p.Tyr321=) rs6828 0.77455
NM_002615.7(SERPINF1):c.440-39C>T rs4274474 0.75763
NM_002615.7(SERPINF1):c.215C>T (p.Thr72Met) rs1136287 0.69033
NM_002615.7(SERPINF1):c.390T>C (p.Thr130=) rs8074840 0.27102
NM_002615.7(SERPINF1):c.440-28C>T rs4274475 0.26633
NM_002615.7(SERPINF1):c.644-14A>T rs3891224 0.12986
NM_002615.7(SERPINF1):c.643+9G>A rs12103559 0.07824
NM_002615.6(SERPINF1):c.-86C>A rs9913583 0.06657
NM_002615.7(SERPINF1):c.395C>G (p.Pro132Arg) rs1804145 0.02133
NM_002615.7(SERPINF1):c.509C>T (p.Thr170Met) rs762383656 0.00002
NM_002615.7(SERPINF1):c.502G>T (p.Val168Phe) rs1597352279
NM_002615.7(SERPINF1):c.85-14C>A rs200755661

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