List of variants in gene combination RAD50, TH2-LCR, TH2LCRR 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.3455G>A (p.Arg1152Gln)	rs144253015	0.00025
NM_005732.4(RAD50):c.3769T>G (p.Ser1257Ala)	rs786201205	0.00008
NM_005732.4(RAD50):c.3496C>T (p.Arg1166Trp)	rs587782577	0.00005
NM_005732.4(RAD50):c.3467G>A (p.Arg1156His)	rs587780156	0.00002
NM_005732.4(RAD50):c.3466C>T (p.Arg1156Cys)	rs535261113	0.00001
NM_005732.4(RAD50):c.3753-4G>T	rs775426160	0.00001
NM_005732.4(RAD50):c.3442C>T (p.Arg1148Cys)	rs746841895
NM_005732.4(RAD50):c.3475+9dup	rs2149862832
NM_005732.4(RAD50):c.3690G>A (p.Leu1230=)	rs1561660969
NM_005732.4(RAD50):c.3766C>A (p.Arg1256Ser)	rs561655417

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