List of variants in gene combination ARHGAP9, MARS1 reported as uncertain significance for Charcot-Marie-Tooth disease axonal type 2U

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_004990.4(MARS1):c.95C>G (p.Thr32Ser)	rs11540809	0.00014
NM_004990.4(MARS1):c.31G>A (p.Gly11Ser)	rs750309467	0.00002
NM_004990.4(MARS1):c.2T>A (p.Met1Lys)	rs760194380	0.00001
NM_004990.4(MARS1):c.70G>A (p.Gly24Ser)	rs1227531274	0.00001
NM_004990.4(MARS1):c.97del (p.Thr32_Val33insTer)	rs773474721	0.00001
NM_004990.4(MARS1):c.109+7GTGCTG[3]	rs763091763
NM_004990.4(MARS1):c.109G>A (p.Asp37Asn)
NM_004990.4(MARS1):c.13G>A (p.Val5Met)	rs587777227
NM_004990.4(MARS1):c.31G>C (p.Gly11Arg)
NM_004990.4(MARS1):c.38T>C (p.Leu13Ser)	rs1875583589
NM_004990.4(MARS1):c.5G>C (p.Arg2Thr)
NM_004990.4(MARS1):c.67C>G (p.Arg23Gly)	rs2139993470
NM_004990.4(MARS1):c.68G>A (p.Arg23Gln)	rs1247809884
NM_004990.4(MARS1):c.71G>C (p.Gly24Ala)
NM_004990.4(MARS1):c.73A>G (p.Arg25Gly)
NM_004990.4(MARS1):c.86T>C (p.Leu29Pro)
NM_004990.4(MARS1):c.89T>G (p.Ile30Ser)

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