ClinVar Miner

List of variants in gene NR3C1 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000176.3(NR3C1):c.879G>A (p.Lys293=) rs10482622 0.02642
NM_000176.3(NR3C1):c.1088A>G (p.Asn363Ser) rs56149945 0.01969
NM_000176.3(NR3C1):c.68G>A (p.Arg23Lys) rs6190 0.01857
NM_000176.3(NR3C1):c.66G>A (p.Glu22=) rs6189 0.01685
NM_000176.3(NR3C1):c.*3550G>A rs10482714 0.01274
NM_000176.3(NR3C1):c.*1880A>G rs10043662 0.00459
NM_001018077.1(NR3C1):c.-620G>A rs61757433 0.00264
NM_001018077.1(NR3C1):c.-616T>G rs61757434 0.00254
NM_000176.3(NR3C1):c.*2042C>T rs13306586 0.00131
NM_000176.3(NR3C1):c.2182-9C>G rs72542757 0.00121
NM_001018077.1(NR3C1):c.-1008C>T rs72555796 0.00081
NM_000176.3(NR3C1):c.*3076C>T rs72542769 0.00066
NM_000176.3(NR3C1):c.*290A>C rs72542758 0.00061
NM_000176.3(NR3C1):c.*3153C>T rs2301177 0.00061
NM_000176.3(NR3C1):c.1242A>G (p.Thr414=) rs67902340 0.00061
NM_000176.3(NR3C1):c.2250C>T (p.Pro750=) rs67300719 0.00061
NM_000176.3(NR3C1):c.897A>G (p.Thr299=) rs13306588 0.00061
NM_000176.3(NR3C1):c.1570A>G (p.Thr524Ala) rs567965061 0.00001
NM_001018077.1(NR3C1):c.-445A>G rs527246890 0.00001
NM_000176.3(NR3C1):c.*1220_*1225dup rs72542761
NM_001018077.1(NR3C1):c.-958G>T rs72555797

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