ClinVar Miner

List of variants in gene MC2R reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000529.2(MC2R):c.*1099A>T rs3888305 0.57649
NM_000529.2(MC2R):c.*685G>A rs4308014 0.56358
NM_000529.2(MC2R):c.*58G>A rs4797825 0.56131
NM_000529.2(MC2R):c.*2394C>G rs1940907 0.55774
NM_000529.2(MC2R):c.*615C>T rs4464147 0.37506
NM_000529.2(MC2R):c.*111G>A rs4797824 0.28031
NM_000529.2(MC2R):c.*1896C>T rs28926188 0.11947
NM_000529.2(MC2R):c.*2138G>T rs3744819 0.10932
NM_000529.2(MC2R):c.*1885T>C rs3760536 0.07937
NM_000529.2(MC2R):c.*880C>T rs28926184 0.03103
NM_000529.2(MC2R):c.833T>G (p.Phe278Cys) rs28926182 0.02378
NM_000529.2(MC2R):c.*2426T>C rs1940906 0.01815
NM_000529.2(MC2R):c.*1759C>A rs35547931 0.01767
NM_000529.2(MC2R):c.*1877A>G rs28926187 0.01558
NM_000529.2(MC2R):c.*491A>G rs28926183 0.01176
NM_000529.2(MC2R):c.*1144G>A rs114107471 0.01117
NM_000529.2(MC2R):c.*1330A>G rs76459561 0.01105
NM_000529.2(MC2R):c.-44G>C rs28926177 0.00804
NM_000529.2(MC2R):c.-90T>C rs35534963 0.00657
NM_000529.2(MC2R):c.-94G>A rs34426564 0.00590
NM_000529.2(MC2R):c.*2528T>G rs150288954 0.00081
NM_000529.2(MC2R):c.*535G>C rs139176501 0.00080
NM_000529.2(MC2R):c.*1061C>A rs117631803
NM_000529.2(MC2R):c.*1604G>C rs28926185
NM_000529.2(MC2R):c.*1920T>A rs28926189

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