List of variants in gene combination DNM2, LOC130063529 reported as uncertain significance for Charcot-Marie-Tooth disease dominant intermediate B

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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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.-116C>T	rs966672075	0.00004
NM_001005361.3(DNM2):c.8A>G (p.Asn3Ser)	rs890297188	0.00003
NM_001005361.3(DNM2):c.149A>G (p.Asn50Ser)	rs757121012	0.00002
NM_001005361.3(DNM2):c.5G>A (p.Gly2Asp)	rs1375606719	0.00002
NM_001005361.3(DNM2):c.-153G>T	rs886054138	0.00001
NM_001005361.3(DNM2):c.10C>T (p.Arg4Cys)	rs1202955393	0.00001
NM_001005361.3(DNM2):c.20A>G (p.Glu7Gly)	rs1435133623	0.00001
NM_001005361.3(DNM2):c.31C>T (p.Pro11Ser)	rs1014814501	0.00001
NM_001005361.3(DNM2):c.83A>T (p.His28Leu)	rs774962668	0.00001
NM_001005361.3(DNM2):c.88G>A (p.Asp30Asn)	rs1344949726	0.00001
NM_001005361.3(DNM2):c.-122G>A	rs886054139
NM_001005361.3(DNM2):c.-19G>T	rs753599004
NM_001005361.3(DNM2):c.-23_12del (p.Met1fs)	rs2512931088
NM_001005361.3(DNM2):c.102C>G (p.Ile34Met)	rs552741402
NM_001005361.3(DNM2):c.104C>T (p.Ala35Val)
NM_001005361.3(DNM2):c.109G>T (p.Val37Leu)	rs2512931662
NM_001005361.3(DNM2):c.126C>A (p.Ala42=)	rs1425173670
NM_001005361.3(DNM2):c.160C>G (p.Arg54Gly)	rs1295054396
NM_001005361.3(DNM2):c.16A>G (p.Met6Val)	rs2068818174
NM_001005361.3(DNM2):c.19G>C (p.Glu7Gln)	rs1008731390
NM_001005361.3(DNM2):c.37G>A (p.Val13Ile)	rs1479865077
NM_001005361.3(DNM2):c.3G>T (p.Met1Ile)	rs2512931214
NM_001005361.3(DNM2):c.41A>G (p.Asn14Ser)	rs2145637630
NM_001005361.3(DNM2):c.54C>A (p.Asp18Glu)	rs2068819294
NM_001005361.3(DNM2):c.65C>G (p.Ser22Cys)	rs2145637734
NM_001005361.3(DNM2):c.70G>A (p.Gly24Ser)	rs2512931490
NM_001005361.3(DNM2):c.77G>C (p.Ser26Thr)	rs2068819966
NM_001005361.3(DNM2):c.79T>G (p.Cys27Gly)	rs2068820028
NM_001005361.3(DNM2):c.90C>G (p.Asp30Glu)	rs759919549
NM_001005361.3(DNM2):c.95C>T (p.Pro32Leu)	rs2145637847

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