List of variants in gene DNMT3A reported as not provided 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_022552.5(DNMT3A):c.1903C>T (p.Arg635Trp)	rs144689354	0.00006
NM_022552.5(DNMT3A):c.2711C>T (p.Pro904Leu)	rs149095705	0.00006
NM_022552.5(DNMT3A):c.2309C>T (p.Ser770Leu)	rs758845779	0.00003
GRCh37/hg19 2p23.3(chr2:25464105-25581265)
NM_022552.5(DNMT3A):c.1004A>G (p.Lys335Arg)	rs2149307214
NM_022552.5(DNMT3A):c.102C>T (p.Gly34=)	rs2465903445
NM_022552.5(DNMT3A):c.1913C>G (p.Ser638Cys)	rs1253868717
NM_022552.5(DNMT3A):c.1978T>C (p.Tyr660His)	rs1674056899
NM_022552.5(DNMT3A):c.2062C>T (p.Arg688Cys)	rs1484795800
Single allele

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