ClinVar Miner

List of variants reported as uncertain significance for Oguchi disease by Illumina Laboratory Services, Illumina

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_000541.5(SAG):c.250C>T (p.Arg84Cys) rs115857633 0.00530
NM_000541.5(SAG):c.525A>G (p.Arg175=) rs199839554 0.00285
NM_000541.5(SAG):c.31G>A (p.Glu11Lys) rs200078242 0.00129
NM_000541.5(SAG):c.*98G>A rs184255686 0.00048
NM_000541.5(SAG):c.473C>A (p.Thr158Lys) rs199537652 0.00034
NM_000541.5(SAG):c.1054G>A (p.Ala352Thr) rs201307508 0.00029
NM_000541.5(SAG):c.1167T>A (p.Asp389Glu) rs199798289 0.00019
NM_000541.5(SAG):c.1132G>A (p.Val378Ile) rs200602069 0.00018
NM_000541.5(SAG):c.453T>G (p.Phe151Leu) rs770558895 0.00014
NM_000541.5(SAG):c.866C>T (p.Ala289Val) rs373460295 0.00009
NM_000541.5(SAG):c.298G>A (p.Ala100Thr) rs771117432 0.00008
NM_000541.5(SAG):c.944+5G>A rs374048703 0.00007
NM_000541.5(SAG):c.468C>T (p.Phe156=) rs375593027 0.00006
NM_000541.5(SAG):c.838A>G (p.Lys280Glu) rs373986650 0.00006
NM_000541.4(SAG):c.-331G>T rs752812406 0.00005
NM_000541.5(SAG):c.*113C>T rs1055247940 0.00005
NM_000541.5(SAG):c.154G>C (p.Asp52His) rs200296556 0.00005
NM_000541.5(SAG):c.269C>G (p.Ser90Cys) rs531041701 0.00003
NM_000541.5(SAG):c.*20C>T rs756466617 0.00002
NM_000541.5(SAG):c.777C>T (p.Tyr259=) rs766104513 0.00002
NM_000541.5(SAG):c.820C>T (p.Pro274Ser) rs369789189 0.00002
NM_000541.5(SAG):c.875G>A (p.Arg292Gln) rs554322769 0.00002
NM_000541.5(SAG):c.-11G>A rs754551985 0.00001
NM_000541.5(SAG):c.-28-10A>G rs1462642188 0.00001
NM_000541.5(SAG):c.208C>T (p.Arg70Cys) rs777934036 0.00001
NM_000541.5(SAG):c.75+7G>T rs753990994 0.00001
NM_000541.5(SAG):c.778G>A (p.Val260Ile) rs1443433091 0.00001
NM_000541.4(SAG):c.-278A>G rs886055799
NM_000541.5(SAG):c.793A>G (p.Met265Val) rs781755716

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