List of variants reported as likely benign for adrenal gland neoplasm by Myriad Genetics, Inc.

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln)	rs607969	0.01309
NM_004168.4(SDHA):c.313-19G>T	rs185555941	0.00235
NM_001370259.2(MEN1):c.-20G>A	rs386134244	0.00158
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr)	rs140736646	0.00060
NM_004168.4(SDHA):c.456+6G>T	rs371735891	0.00047
NM_004168.4(SDHA):c.622-8T>C	rs370714378	0.00037
NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp)	rs375804228	0.00015
NM_001370259.2(MEN1):c.1506G>C (p.Lys502Asn)	rs774296730	0.00014
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly)	rs191412461	0.00013
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu)	rs141679530	0.00011
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp)	rs143329068	0.00009
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.1391C>T (p.Ala464Val)	rs778728934	0.00007
NM_003001.5(SDHC):c.179+10G>A	rs532455044	0.00006
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp)	rs149383809	0.00004
NM_004168.4(SDHA):c.1432+7G>C	rs760526397	0.00004
NM_004168.4(SDHA):c.456+9C>T	rs200565489	0.00004
NM_001370259.2(MEN1):c.1350+6G>A	rs746077651	0.00002
NM_001370259.2(MEN1):c.784-16C>T	rs754257177	0.00002
NM_001370259.2(MEN1):c.1350+3G>A
NM_001370259.2(MEN1):c.61C>A (p.Arg21Ser)	rs541476418
NM_004168.4(SDHA):c.-7A>C	rs751633537
NM_004168.4(SDHA):c.830C>T (p.Thr277Met)	rs367721665

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