List of variants in gene DCHS1 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003737.4(DCHS1):c.4215T>C (p.Leu1405=)	rs2659872	0.52121
NM_003737.4(DCHS1):c.3696G>A (p.Pro1232=)	rs2659871	0.44455
NM_003737.4(DCHS1):c.1986+17A>T	rs2659869	0.39478
NM_003737.4(DCHS1):c.1902C>T (p.His634=)	rs997263	0.35112
NM_003737.4(DCHS1):c.6365-11A>G	rs11827437	0.34333
NM_003737.4(DCHS1):c.5846C>T (p.Thr1949Met)	rs4758443	0.30888
NM_003737.4(DCHS1):c.7147-9A>G	rs10458926	0.16006
NM_003737.4(DCHS1):c.6991G>A (p.Val2331Ile)	rs7924553	0.03864
NM_003737.4(DCHS1):c.3798G>A (p.Leu1266=)	rs12292546	0.03188
NM_003737.4(DCHS1):c.7839G>A (p.Glu2613=)	rs2659876	0.01574
NM_003737.4(DCHS1):c.8196C>T (p.Asp2732=)	rs74850790	0.00816
NM_003737.4(DCHS1):c.1245C>A (p.Ser415Arg)	rs117368891	0.00644
NM_003737.4(DCHS1):c.1058G>A (p.Arg353Gln)	rs139223913	0.00138
NM_003737.4(DCHS1):c.7428C>T (p.Asn2476=)

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