List of variants in gene DISP1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001377229.1(DISP1):c.3822A>C (p.Pro1274=)	rs9441941	0.53617
NM_001377229.1(DISP1):c.890-14T>C	rs2609359	0.34985
NM_001377229.1(DISP1):c.2835A>G (p.Lys945=)	rs2609355	0.26356
NM_001377229.1(DISP1):c.307G>A (p.Glu103Lys)	rs2609383	0.15673
NM_001377229.1(DISP1):c.309G>T (p.Glu103Asp)	rs2789975	0.15672
NM_001377229.1(DISP1):c.3273C>T (p.Phe1091=)	rs149359302	0.00784
NM_001377229.1(DISP1):c.3287T>C (p.Met1096Thr)	rs144673025	0.00523
NM_001377229.1(DISP1):c.3716T>C (p.Leu1239Pro)	rs115615723	0.00375
NM_001377229.1(DISP1):c.2439T>C (p.Asp813=)	rs147223870	0.00239

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