List of variants in gene SDHA reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 99

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_004168.4(SDHA):c.955A>C (p.Ile319Leu)	rs377509915	0.00016
NM_004168.4(SDHA):c.704T>C (p.Ile235Thr)	rs144513891	0.00015
NM_004168.4(SDHA):c.991G>A (p.Ala331Thr)	rs200526913	0.00014
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly)	rs191412461	0.00013
NM_004168.4(SDHA):c.205G>A (p.Ala69Thr)	rs370481102	0.00012
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln)	rs199844384	0.00009
NM_004168.4(SDHA):c.1591G>A (p.Val531Met)	rs371056571	0.00009
NM_004168.4(SDHA):c.1661G>A (p.Arg554Gln)	rs376391115	0.00009
NM_004168.4(SDHA):c.1532T>C (p.Leu511Pro)	rs375194444	0.00008
NM_004168.4(SDHA):c.1597C>G (p.Gln533Glu)	rs149367009	0.00008
NM_004168.4(SDHA):c.-5C>T	rs572126995	0.00006
NM_004168.4(SDHA):c.1064+5G>A	rs200021115	0.00006
NM_004168.4(SDHA):c.994C>G (p.Pro332Ala)	rs373509391	0.00006
NM_004168.4(SDHA):c.1001C>T (p.Ala334Val)	rs765180271	0.00004
NM_004168.4(SDHA):c.1115C>G (p.Pro372Arg)	rs141493530	0.00004
NM_004168.4(SDHA):c.1724C>T (p.Ala575Val)	rs750327309	0.00004
NM_004168.4(SDHA):c.1771G>A (p.Ala591Thr)	rs1042170	0.00004
NM_004168.4(SDHA):c.1930G>A (p.Val644Met)	rs3211483	0.00004
NM_004168.4(SDHA):c.1951G>A (p.Glu651Lys)	rs375396913	0.00004
NM_004168.4(SDHA):c.1973C>T (p.Pro658Leu)	rs377632619	0.00004
NM_004168.4(SDHA):c.563G>A (p.Arg188Gln)	rs139881415	0.00004
NM_004168.4(SDHA):c.5C>T (p.Ser2Leu)	rs780064103	0.00004
NM_004168.4(SDHA):c.1573G>A (p.Val525Met)	rs979815942	0.00003
NM_004168.4(SDHA):c.1794+3G>C	rs375883981	0.00003
NM_004168.4(SDHA):c.1936G>A (p.Asp646Asn)	rs376986935	0.00003
NM_004168.4(SDHA):c.424A>G (p.Met142Val)	rs776848209	0.00003
NM_004168.4(SDHA):c.454G>A (p.Glu152Lys)	rs778737664	0.00003
NM_004168.4(SDHA):c.607A>G (p.Thr203Ala)	rs373340696	0.00003
NM_004168.4(SDHA):c.613T>C (p.Tyr205His)	rs61754481	0.00003
NM_004168.4(SDHA):c.109G>A (p.Val37Ile)	rs758426529	0.00002
NM_004168.4(SDHA):c.1394G>A (p.Arg465Gln)	rs138277996	0.00002
NM_004168.4(SDHA):c.1657G>A (p.Asp553Asn)	rs769882609	0.00002
NM_004168.4(SDHA):c.1679C>T (p.Thr560Met)	rs775350508	0.00002
NM_004168.4(SDHA):c.1799G>A (p.Arg600Gln)	rs1126568	0.00002
NM_004168.4(SDHA):c.464A>G (p.Asn155Ser)	rs749824479	0.00002
NM_004168.4(SDHA):c.1122G>T (p.Glu374Asp)	rs377283167	0.00001
NM_004168.4(SDHA):c.1127T>C (p.Leu376Pro)	rs1433477205	0.00001
NM_004168.4(SDHA):c.1196C>A (p.Pro399Gln)	rs878854625	0.00001
NM_004168.4(SDHA):c.1234G>A (p.Gly412Ser)	rs768055345	0.00001
NM_004168.4(SDHA):c.1300G>A (p.Gly434Ser)	rs529198317	0.00001
NM_004168.4(SDHA):c.1340A>G (p.His447Arg)	rs779151375	0.00001
NM_004168.4(SDHA):c.1429C>T (p.Pro477Ser)	rs770506764	0.00001
NM_004168.4(SDHA):c.150+1G>A	rs1057523165	0.00001
NM_004168.4(SDHA):c.1579C>T (p.Arg527Cys)	rs138723511	0.00001
NM_004168.4(SDHA):c.1787A>G (p.Asp596Gly)	rs1126557	0.00001
NM_004168.4(SDHA):c.1795-3C>G	rs544544409	0.00001
NM_004168.4(SDHA):c.1798C>T (p.Arg600Trp)	rs878854630	0.00001
NM_004168.4(SDHA):c.1915C>G (p.Leu639Val)	rs1126697	0.00001
NM_004168.4(SDHA):c.23C>G (p.Ser8Trp)	rs878854631	0.00001
NM_004168.4(SDHA):c.260C>T (p.Thr87Ile)	rs756543943	0.00001
NM_004168.4(SDHA):c.466T>G (p.Tyr156Asp)	rs569384870	0.00001
NM_004168.4(SDHA):c.666G>T (p.Leu222Phe)	rs778256616	0.00001
NM_004168.4(SDHA):c.694C>T (p.Arg232Cys)	rs878854635	0.00001
NM_004168.4(SDHA):c.707C>T (p.Ala236Val)	rs1060503703	0.00001
NM_004168.4(SDHA):c.776A>G (p.Tyr259Cys)	rs1579397049	0.00001
NM_004168.4(SDHA):c.812C>G (p.Thr271Ser)	rs765611464	0.00001
NM_004168.4(SDHA):c.86G>A (p.Gly29Glu)	rs1436200566	0.00001
NM_004168.4(SDHA):c.914G>A (p.Cys305Tyr)	rs878854638	0.00001
NM_004168.4(SDHA):c.92G>A (p.Arg31Gln)	rs752532780	0.00001
NM_004168.4(SDHA):c.986G>A (p.Arg329Gln)	rs138265892	0.00001
NM_004168.4(SDHA):c.-1C>T	rs560932680
NM_004168.4(SDHA):c.106A>G (p.Thr36Ala)	rs750500173
NM_004168.4(SDHA):c.1171G>C (p.Ala391Pro)	rs376597185
NM_004168.4(SDHA):c.1261-5delinsGAAA	rs1553999701
NM_004168.4(SDHA):c.1272C>G (p.His424Gln)	rs754805626
NM_004168.4(SDHA):c.1273G>A (p.Val425Met)	rs201822097
NM_004168.4(SDHA):c.1342G>A (p.Gly448Ser)	rs1064795863
NM_004168.4(SDHA):c.1354C>T (p.Leu452Phe)	rs1064796477
NM_004168.4(SDHA):c.13C>T (p.Arg5Trp)	rs770866830
NM_004168.4(SDHA):c.1403C>A (p.Ala468Asp)	rs1057524636
NM_004168.4(SDHA):c.1428G>T (p.Arg476Ser)	rs377415114
NM_004168.4(SDHA):c.145G>C (p.Asp49His)	rs1734836072
NM_004168.4(SDHA):c.1547A>G (p.Gln516Arg)	rs981171929
NM_004168.4(SDHA):c.1556T>A (p.Met519Lys)
NM_004168.4(SDHA):c.1568C>G (p.Ala523Gly)	rs1736785630
NM_004168.4(SDHA):c.1609G>C (p.Gly537Arg)
NM_004168.4(SDHA):c.1795G>A (p.Val599Met)
NM_004168.4(SDHA):c.1835G>A (p.Gly612Glu)	rs1057523336
NM_004168.4(SDHA):c.1842G>C (p.Gln614His)	rs2126641413
NM_004168.4(SDHA):c.1864T>C (p.Trp622Arg)	rs1554002480
NM_004168.4(SDHA):c.1886A>G (p.Tyr629Cys)	rs6960
NM_004168.4(SDHA):c.1894G>T (p.Val632Phe)	rs369639811
NM_004168.4(SDHA):c.1930_1932delinsATA (p.Val644Ile)
NM_004168.4(SDHA):c.1984C>T (p.Arg662Cys)	rs1737195067
NM_004168.4(SDHA):c.1985G>A (p.Arg662His)	rs1042457
NM_004168.4(SDHA):c.1985G>C (p.Arg662Pro)
NM_004168.4(SDHA):c.263C>G (p.Ala88Gly)	rs1734891785
NM_004168.4(SDHA):c.44G>A (p.Arg15His)
NM_004168.4(SDHA):c.456G>A (p.Glu152=)	rs1579384590
NM_004168.4(SDHA):c.518T>C (p.Phe173Ser)
NM_004168.4(SDHA):c.63+3G>C	rs2126522872
NM_004168.4(SDHA):c.749A>G (p.Lys250Arg)	rs1060503700
NM_004168.4(SDHA):c.771-21_771-13del
NM_004168.4(SDHA):c.830C>T (p.Thr277Met)	rs367721665
NM_004168.4(SDHA):c.833C>T (p.Ala278Val)	rs1057523490
NM_004168.4(SDHA):c.905G>A (p.Gly302Asp)	rs1735544082
NM_004168.4(SDHA):c.934C>T (p.Arg312Cys)	rs1735549033
NM_004168.4(SDHA):c.992C>T (p.Ala331Val)	rs1206201147

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