List of variants in gene ZSWIM6 studied for bone development disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_020928.2(ZSWIM6):c.1906G>A (p.Val636Met)	rs140760439	0.00337
NM_020928.2(ZSWIM6):c.1722C>T (p.Asp574=)	rs187525163	0.00290
NM_020928.2(ZSWIM6):c.1472A>G (p.Asn491Ser)	rs201912422	0.00048
NM_020928.2(ZSWIM6):c.1991T>C (p.Met664Thr)	rs371478900	0.00008
NM_020928.2(ZSWIM6):c.31G>A (p.Ala11Thr)	rs1038709799	0.00006
NM_020928.2(ZSWIM6):c.1781A>G (p.Asn594Ser)	rs1257102056	0.00001
NM_020928.2(ZSWIM6):c.2281C>T (p.Arg761Trp)	rs756935198	0.00001
NM_020928.2(ZSWIM6):c.151GCG[7] (p.Ala56dup)	rs779283808
NM_020928.2(ZSWIM6):c.1760G>C (p.Arg587Thr)
NM_020928.2(ZSWIM6):c.2248G>A (p.Gly750Arg)
NM_020928.2(ZSWIM6):c.3487C>T (p.Arg1163Trp)	rs587777695
NM_020928.2(ZSWIM6):c.440_454del (p.Ala147_Gly151del)	rs772099709
NM_020928.2(ZSWIM6):c.498A>G (p.Ala166=)	rs964738831
NM_020928.2(ZSWIM6):c.683A>G (p.His228Arg)	rs1747601529
NM_020928.2(ZSWIM6):c.79_96dup (p.Ser27_Gly32dup)	rs1554028299

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