ClinVar Miner

List of variants reported as benign for Warburg micro syndrome 1

Included ClinVar conditions (2):
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ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_012233.3(RAB3GAP1):c.2265T>C (p.Phe755=) rs17261772 0.53257
NM_012233.3(RAB3GAP1):c.1793A>G (p.Asn598Ser) rs10445686 0.14088
NM_012233.3(RAB3GAP1):c.*1077T>C rs16831395 0.06295
NM_012233.3(RAB3GAP1):c.*1378T>C rs59746814 0.04762
NM_012233.3(RAB3GAP1):c.*171G>A rs11558413 0.04215
NM_012233.3(RAB3GAP1):c.1992G>A (p.Ser664=) rs7595725 0.02952
NM_012233.3(RAB3GAP1):c.*135C>G rs10170125 0.02787
NM_012233.3(RAB3GAP1):c.1041A>G (p.Arg347=) rs77972211 0.01269
NM_012233.3(RAB3GAP1):c.*995T>C rs116237324 0.01076
NM_012233.3(RAB3GAP1):c.357A>G (p.Val119=) rs73959261 0.01043
NM_012233.3(RAB3GAP1):c.2463C>T (p.Phe821=) rs61748693 0.00825
NM_012233.3(RAB3GAP1):c.669G>T (p.Leu223Phe) rs76927619 0.00770
NM_012233.3(RAB3GAP1):c.*992G>A rs11558414 0.00645
NM_012233.3(RAB3GAP1):c.913A>G (p.Ile305Val) rs116775947 0.00602
NM_012233.3(RAB3GAP1):c.*1826G>C rs114264557 0.00318
NM_012233.3(RAB3GAP1):c.*404C>T rs149483456 0.00180
NM_012233.3(RAB3GAP1):c.2800C>G (p.Pro934Ala) rs77535003

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