List of variants in gene MESP2 reported as benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001039958.2(MESP2):c.*431C>T	rs11073889	0.62378
NM_001039958.2(MESP2):c.573G>A (p.Gly191=)	rs113097169	0.13255
NM_001039958.2(MESP2):c.412G>A (p.Val138Met)	rs28462216	0.06491
NM_001039958.2(MESP2):c.558G>A (p.Gln186=)	rs28546919	0.05106
NM_001039958.2(MESP2):c.531G>A (p.Ala177=)	rs75049807	0.04869
NM_001039958.2(MESP2):c.671C>T (p.Ser224Phe)	rs71647807	0.02596
NM_001039958.2(MESP2):c.717G>C (p.Gly239=)	rs181559095	0.00329
NM_001039958.2(MESP2):c.67G>A (p.Gly23Ser)	rs548112443	0.00101
NM_001039958.2(MESP2):c.185G>A (p.Arg62Gln)	rs566641514	0.00041
NM_001039958.2(MESP2):c.408G>T (p.Ser136=)	rs760746152	0.00011
NM_001039958.1(MESP2):c.535GGGCAGGGGCAA[2_4]	rs397507446
NM_001039958.2(MESP2):c.197C>G (p.Ala66Gly)	rs71647809
NM_001039958.2(MESP2):c.498C>A (p.Pro166=)	rs200336355
NM_001039958.2(MESP2):c.498C>G (p.Pro166=)	rs200336355
NM_001039958.2(MESP2):c.534GGGGCAGGGGCAAGGGCAGGGGCA[1] (p.180QG[9])	rs200021459
NM_001039958.2(MESP2):c.549_584del (p.180_181QG[7])	rs749710849
NM_001039958.2(MESP2):c.552GGGGCA[1] (p.180QG[11])	rs56192595
NM_001039958.2(MESP2):c.670T>C (p.Ser224Pro)	rs118204033

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