ClinVar Miner

List of variants in gene MEGF10 reported as uncertain significance by GeneDx

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001256545.2(MEGF10):c.259A>G (p.Met87Val) rs41298304 0.00052
NM_001256545.2(MEGF10):c.452G>A (p.Arg151Gln) rs78069165 0.00039
NM_001256545.2(MEGF10):c.1622G>T (p.Arg541Leu) rs142664089 0.00035
NM_001256545.2(MEGF10):c.50G>A (p.Cys17Tyr) rs145733370 0.00023
NM_001256545.2(MEGF10):c.877A>G (p.Thr293Ala) rs144187055 0.00022
NM_001256545.2(MEGF10):c.3170G>A (p.Arg1057Lys) rs374156507 0.00015
NM_001256545.2(MEGF10):c.401A>G (p.Asn134Ser) rs574376262 0.00013
NM_001256545.2(MEGF10):c.1726C>T (p.Arg576Cys) rs143087353 0.00009
NM_001256545.2(MEGF10):c.1959C>T (p.Gly653=) rs146017981 0.00006
NM_001256545.2(MEGF10):c.2857-2A>G rs199750143 0.00006
NM_001256545.2(MEGF10):c.451C>T (p.Arg151Trp) rs767672691 0.00006
NM_001256545.2(MEGF10):c.2330G>A (p.Arg777His) rs565304206 0.00005
NM_001256545.2(MEGF10):c.2590A>G (p.Ile864Val) rs780877446 0.00004
NM_001256545.2(MEGF10):c.2942C>T (p.Pro981Leu) rs1064793648 0.00004
NM_001256545.2(MEGF10):c.212G>A (p.Arg71Gln) rs886059862 0.00003
NM_001256545.2(MEGF10):c.2150A>G (p.Asn717Ser) rs116135607 0.00003
NM_001256545.2(MEGF10):c.2864A>C (p.Asn955Thr) rs1353393054 0.00003
NM_001256545.2(MEGF10):c.952G>A (p.Val318Ile) rs959864264 0.00002
NM_001256545.2(MEGF10):c.1322C>T (p.Thr441Ile) rs1160030961 0.00001
NM_001256545.2(MEGF10):c.1523A>G (p.Asn508Ser) rs184606767 0.00001
NM_001256545.2(MEGF10):c.1801G>A (p.Glu601Lys) rs778255998 0.00001
NM_001256545.2(MEGF10):c.2576T>C (p.Ile859Thr) rs895294556 0.00001
NM_001256545.2(MEGF10):c.3055A>G (p.Ser1019Gly) rs1766320871 0.00001
NM_001256545.2(MEGF10):c.3278G>A (p.Arg1093His) rs187800437 0.00001
NM_001256545.2(MEGF10):c.529C>T (p.Arg177Cys) rs748641801 0.00001
NM_001256545.2(MEGF10):c.935C>T (p.Pro312Leu) rs199702225 0.00001
NM_001256545.2(MEGF10):c.1075C>T (p.Leu359Phe) rs754958105
NM_001256545.2(MEGF10):c.1099C>T (p.Arg367Trp)
NM_001256545.2(MEGF10):c.1292C>T (p.Ala431Val) rs1057518319
NM_001256545.2(MEGF10):c.1643A>T (p.Asp548Val) rs1338867391
NM_001256545.2(MEGF10):c.2363A>G (p.Lys788Arg) rs1200074021
NM_001256545.2(MEGF10):c.2742C>A (p.His914Gln) rs2127029173
NM_001256545.2(MEGF10):c.2743A>C (p.Ser915Arg) rs1387603431
NM_001256545.2(MEGF10):c.2785A>T (p.Ser929Cys) rs1561653221
NM_001256545.2(MEGF10):c.2819C>T (p.Pro940Leu) rs1765999410
NM_001256545.2(MEGF10):c.3272A>G (p.Asn1091Ser)
NM_001256545.2(MEGF10):c.3331T>C (p.Tyr1111His) rs1064795277
NM_001256545.2(MEGF10):c.3415_3417dup (p.Ser1139dup) rs2127049632
NM_001256545.2(MEGF10):c.733G>T (p.Val245Leu) rs755790851

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