List of variants in gene WNT1 reported as uncertain significance for bone disorder

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005430.4(WNT1):c.1007C>T (p.Thr336Met)	rs148154047	0.00294
NM_005430.4(WNT1):c.754G>C (p.Gly252Arg)	rs200151492	0.00067
NM_005430.4(WNT1):c.535C>T (p.Leu179Phe)	rs377240313	0.00013
NM_005430.4(WNT1):c.506G>A (p.Gly169Asp)	rs371672410	0.00009
NM_005430.4(WNT1):c.27C>T (p.Gly9=)	rs772782141	0.00001
NM_005430.4(WNT1):c.689G>A (p.Arg230His)	rs560459579	0.00001
NM_005430.4(WNT1):c.1060del (p.His354fs)	rs1233798164
NM_005430.4(WNT1):c.1090C>G (p.Arg364Gly)	rs1435433748
NM_005430.4(WNT1):c.23C>T (p.Pro8Leu)	rs1219729580
NM_005430.4(WNT1):c.501G>C (p.Trp167Cys)	rs1592257435
NM_005430.4(WNT1):c.625-5C>T	rs1207715560
NM_005430.4(WNT1):c.937C>A (p.Arg313Ser)	rs1162097828
NM_005430.4(WNT1):c.989G>A (p.Cys330Tyr)	rs1565722031

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