ClinVar Miner

List of variants in gene combination GAREM2, HADHA reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000182.5(HADHA):c.1621-26G>T rs1865324 0.82473
NM_000182.5(HADHA):c.1393-62A>C rs13387855 0.82463
NM_000182.5(HADHA):c.*302G>A rs1049987 0.17222
NM_000182.5(HADHA):c.*510A>T rs13432453 0.04522
NM_000182.5(HADHA):c.1392+10G>A rs60085478 0.02277
NM_000182.5(HADHA):c.1620+11G>C rs112236946 0.01807
NM_000182.5(HADHA):c.*561C>T rs115151034 0.00544
NM_000182.5(HADHA):c.*331T>C rs189483687 0.00500
NM_000182.5(HADHA):c.1981C>T (p.Leu661=) rs142348718 0.00450
NM_000182.5(HADHA):c.1690-6G>A rs111662358 0.00412
NM_000182.5(HADHA):c.2146+16T>C rs145930159 0.00408
NM_000182.5(HADHA):c.1843A>G (p.Asn615Asp) rs61731155 0.00349
NM_000182.5(HADHA):c.2060T>C (p.Met687Thr) rs149632783 0.00173
NM_000182.5(HADHA):c.2146+18G>A rs200961004 0.00017
NM_000182.5(HADHA):c.1690-14C>T rs142401180 0.00013
NM_000182.5(HADHA):c.1690-12C>T rs369641464 0.00011
NM_000182.5(HADHA):c.1284C>T (p.Asn428=) rs199535840 0.00009
NM_000182.5(HADHA):c.*202G>A rs7260
NM_000182.5(HADHA):c.1393-10dup rs2147756168
NM_000182.5(HADHA):c.1620+8dup

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