List of variants in gene combination NR0B2, NUDC reported as uncertain significance for not provided

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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_021969.3(NR0B2):c.343C>T (p.Pro115Ser)	rs140901243	0.00059
NM_021969.3(NR0B2):c.160C>T (p.Arg54Cys)	rs113654931	0.00026
NM_021969.3(NR0B2):c.553G>A (p.Ala185Thr)	rs199619628	0.00006
NM_021969.3(NR0B2):c.203C>T (p.Ala68Val)	rs202150278	0.00005
NM_021969.3(NR0B2):c.55G>A (p.Ala19Thr)	rs746657025	0.00002
NM_021969.3(NR0B2):c.121T>C (p.Cys41Arg)	rs569477682	0.00001
NM_021969.3(NR0B2):c.749T>C (p.Leu250Pro)	rs1258917303	0.00001
NM_021969.3(NR0B2):c.100C>G (p.Arg34Gly)	rs74315349
NM_021969.3(NR0B2):c.106C>T (p.Arg36Cys)
NM_021969.3(NR0B2):c.134G>A (p.Arg45Gln)	rs150546920
NM_021969.3(NR0B2):c.157_166del (p.His53fs)	rs540387719
NM_021969.3(NR0B2):c.250C>G (p.Gln84Glu)	rs1327866399
NM_021969.3(NR0B2):c.278G>A (p.Gly93Asp)	rs2082043108
NM_021969.3(NR0B2):c.389G>C (p.Gly130Ala)	rs773062003
NM_021969.3(NR0B2):c.434C>T (p.Ala145Val)	rs778073494
NM_021969.3(NR0B2):c.703C>T (p.Leu235Phe)
NM_021969.3(NR0B2):c.754del (p.Asp252fs)	rs2522569538

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