ClinVar Miner

List of variants in gene SDHD reported as likely benign for adrenal gland disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_003002.4(SDHD):c.*186A>G rs183918321
NM_003002.4(SDHD):c.*352C>G rs192900956
NM_003002.4(SDHD):c.*428A>G rs184654032
NM_003002.4(SDHD):c.*622A>G rs142510105
NM_003002.4(SDHD):c.*663A>G rs200264243
NM_003002.4(SDHD):c.114A>G (p.Arg38=) rs1555186794
NM_003002.4(SDHD):c.141G>A (p.Gln47=) rs1217254088
NM_003002.4(SDHD):c.149A>G (p.His50Arg) rs11214077
NM_003002.4(SDHD):c.159G>A (p.Pro53=) rs201368675
NM_003002.4(SDHD):c.170-10C>T rs952278127
NM_003002.4(SDHD):c.18G>A (p.Arg6=) rs200895313
NM_003002.4(SDHD):c.19C>T (p.Leu7=) rs1337542194
NM_003002.4(SDHD):c.21G>A (p.Leu7=) rs974401612
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289
NM_003002.4(SDHD):c.270G>A (p.Ala90=) rs766656463
NM_003002.4(SDHD):c.270G>C (p.Ala90=) rs766656463
NM_003002.4(SDHD):c.27C>A (p.Ala9=) rs1555186670
NM_003002.4(SDHD):c.282C>G (p.Ser94=) rs781182616
NM_003002.4(SDHD):c.282C>T (p.Ser94=) rs781182616
NM_003002.4(SDHD):c.297C>T (p.Leu99=) rs749657880
NM_003002.4(SDHD):c.312C>T (p.His104=) rs61734352
NM_003002.4(SDHD):c.314+8T>C rs199645781
NM_003002.4(SDHD):c.315-9T>G rs911853469
NM_003002.4(SDHD):c.318C>A (p.Gly106=) rs878854592
NM_003002.4(SDHD):c.342T>C (p.Tyr114=) rs1050032491
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser) rs34677591
NM_003002.4(SDHD):c.405C>A (p.Thr135=) rs1555187606
NM_003002.4(SDHD):c.42A>G (p.Leu14=) rs878854593
NM_003002.4(SDHD):c.435C>T (p.His145=) rs200062830
NM_003002.4(SDHD):c.53-6C>T rs757454290
NM_003002.4(SDHD):c.53C>T (p.Ala18Val) rs192332761
NM_003002.4(SDHD):c.57G>A (p.Leu19=) rs560625389
NM_003002.4(SDHD):c.9T>A (p.Val3=) rs1555186657

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