ClinVar Miner

List of variants in gene combination MAP3K15, PDHA1 reported as benign for carbohydrate metabolism disease

Included ClinVar conditions (304):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_000284.4(PDHA1):c.*1394C>T rs55856360 0.22991
NM_000284.4(PDHA1):c.*1059G>A rs15816 0.22867
NM_000284.4(PDHA1):c.*844A>G rs1042453 0.22833
NM_000284.4(PDHA1):c.*728C>T rs1042452 0.22767
NM_000284.4(PDHA1):c.*1377G>A rs56039350 0.20892
NM_000284.4(PDHA1):c.*614G>T rs5955761 0.06313
NM_000284.4(PDHA1):c.*1598G>C rs11094770 0.06012
NM_000284.4(PDHA1):c.*1563C>G rs7883708 0.01025
NM_000284.4(PDHA1):c.*1682T>C rs55744630 0.00998
NM_000284.4(PDHA1):c.*1869G>C rs15943 0.00434
NM_000284.4(PDHA1):c.*1208A>C rs369499936 0.00252
NM_000284.4(PDHA1):c.*857A>G rs182836908 0.00208
NM_000284.4(PDHA1):c.*864G>A rs192450087 0.00203
NM_000284.4(PDHA1):c.*1345A>G rs193253848 0.00110
NM_000284.4(PDHA1):c.*707G>A rs150945967 0.00012
NM_000284.4(PDHA1):c.*1450C>T rs747229060 0.00011
NM_000284.4(PDHA1):c.*1013C>A rs1042456
NM_000284.4(PDHA1):c.*525C>G rs778207227

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