List of variants reported as uncertain significance for CODAS syndrome

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Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_004793.4(LONP1):c.1817C>T (p.Ala606Val)	rs145519500	0.00100
NM_004793.4(LONP1):c.1985T>G (p.Val662Gly)	rs144822855	0.00069
NM_004793.4(LONP1):c.1600C>T (p.Arg534Cys)	rs150732086	0.00040
NM_004793.4(LONP1):c.1612C>T (p.Arg538Cys)	rs201664019	0.00020
NM_004793.4(LONP1):c.1925C>T (p.Thr642Met)	rs371606894	0.00019
NM_004793.4(LONP1):c.2542G>A (p.Ala848Thr)	rs147591431	0.00019
NM_004793.4(LONP1):c.2203G>A (p.Val735Met)	rs200317240	0.00018
NM_004793.4(LONP1):c.296G>A (p.Gly99Asp)	rs747867148	0.00014
NM_004793.4(LONP1):c.686C>T (p.Ala229Val)	rs80050321	0.00014
NM_004793.4(LONP1):c.325A>G (p.Ile109Val)	rs141593936	0.00013
NM_004793.4(LONP1):c.796C>G (p.Leu266Val)	rs373284466	0.00013
NM_004793.4(LONP1):c.788C>T (p.Thr263Ile)	rs139791767	0.00011
NM_004793.4(LONP1):c.1438C>G (p.Leu480Val)	rs1392705083	0.00003
NM_004793.4(LONP1):c.2482C>T (p.His828Tyr)	rs766992987	0.00002
NM_004793.4(LONP1):c.2812C>T (p.His938Tyr)	rs766783227	0.00002
NM_004793.4(LONP1):c.1939G>A (p.Glu647Lys)	rs149596661	0.00001
NM_004793.4(LONP1):c.2191G>A (p.Glu731Lys)	rs768949488	0.00001
NM_004793.4(LONP1):c.2536G>A (p.Glu846Lys)	rs752945140	0.00001
NM_004793.4(LONP1):c.2716G>T (p.Gly906Trp)	rs775882355	0.00001
NM_004793.4(LONP1):c.44G>C (p.Arg15Pro)	rs2055414315	0.00001
NM_004793.4(LONP1):c.11G>A (p.Ser4Asn)
NM_004793.4(LONP1):c.1409G>T (p.Trp470Leu)	rs2512399718
NM_004793.4(LONP1):c.1913C>T (p.Thr638Met)	rs757666530
NM_004793.4(LONP1):c.2365G>A (p.Asp789Asn)
NM_004793.4(LONP1):c.2422G>A (p.Glu808Lys)	rs1568310102
NM_004793.4(LONP1):c.488A>C (p.Tyr163Ser)	rs2055279214
NM_004793.4(LONP1):c.64_90del (p.Pro22_Arg30del)	rs1355376280
NM_004793.4(LONP1):c.889G>A (p.Val297Met)	rs1599470758

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