ClinVar Miner

List of variants reported as likely benign for adrenal gland neoplasm by Counsyl

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_004168.4(SDHA):c.1664-24del rs534296796 0.00297
NM_004168.4(SDHA):c.146A>G (p.Asp49Gly) rs80207011 0.00261
NM_004168.4(SDHA):c.313-19G>T rs185555941 0.00235
NM_003000.3(SDHB):c.32G>A (p.Arg11His) rs111430410 0.00185
NM_001370259.2(MEN1):c.-20G>A rs386134244 0.00158
NM_001370259.2(MEN1):c.30G>T (p.Leu10=) rs371192390 0.00111
NM_003000.3(SDHB):c.287-26A>G rs201397253 0.00040
NM_003001.5(SDHC):c.20+22G>C rs182261879 0.00032
NM_003001.5(SDHC):c.405+23C>T rs373731336 0.00026
NM_004168.4(SDHA):c.895+13G>A rs201461936 0.00025
NM_003000.3(SDHB):c.642+17T>C rs200597595 0.00016
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu) rs750112288 0.00012
NM_001370259.2(MEN1):c.339C>T (p.Ser113=) rs559635859 0.00011
NM_001370259.2(MEN1):c.492C>T (p.Ala164=) rs146759807 0.00010
NM_001370259.2(MEN1):c.655-4del rs748005956 0.00009
NM_003001.5(SDHC):c.179+10G>A rs532455044 0.00006
NM_004168.4(SDHA):c.1432+7G>C rs760526397 0.00004
NM_004168.4(SDHA):c.456+9C>T rs200565489 0.00004
NM_004168.4(SDHA):c.513T>C (p.Arg171=) rs765157205 0.00004
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=) rs587780841 0.00003
NM_001370259.2(MEN1):c.784-16C>T rs754257177 0.00002
NM_003000.3(SDHB):c.765+13G>A rs115561881 0.00002
NM_001370259.2(MEN1):c.655-5dup rs772016629
NM_003000.3(SDHB):c.424-14_424-9dup rs1064794554
NM_004168.4(SDHA):c.1432+20G>C rs200127852

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